Thursday, June 26, 2008

DRUGS --D

Dactinomycin

Trade Name(s): Cosmegen

Pregnancy Category: C

Medical Category: Antineoplastic

Accepted Indications: Ewing's sarcoma, trophoblastic tumors, various carcinomas, Wilms' tumor, rhabdomyosarcoma, Kaposi's sarcoma, osteosarcoma, malignant melanoma, sarcoma botryoides

Unaccepted Indications: Infectious diseases

Mechanism of Action: May bind with DNA by intercalation

Absorption/Distribution: Does not cross blood-brain barrier

Half life: 36 h

Metabolism: Minimal

Elimination: Biliary, fecal, renal

Adult Dosage: IV, 10–{endash}15 m{mu}g/kg/d for maximum of 5 d every 4–{endash}6 w

Elderly Dosage: Same as adult dose

Child Dosage: Same as adult dose

Infant Dosage: Not recommended

Dosage Forms: Injection: 0.5 mg

Warnings: Do not expose to skin

Frequent Side Effects: Skin darkening, acne, anemia, GI, ulceration, leukopenia, thrombocytopenia, ulcerative stomatitis, nausea, vomiting, skin redness, unusual tiredness

Occasional Side Effects: Hair loss

Rare Side Effects: Bone marrow depression, anaphylaxis, phlebitis, hepatotoxicity, hyperuricemia

Contraindications: Bone marrow depression, chickenpox, herpes zoster

Disease States: Infection, liver impairment

Other Drugs: Radiation therapy, probenecid, sulfinpyrazone, bone marrow depressants, live virus vaccines

Lab Tests: Hemocrit, platelet count

Danazol

Trade Name(s): Danocrine

Chemically Related To: Androgens

Pregnancy Category: X

Medical Category: Gonadotropin inhibition

Accepted Indications: Endometriosis, fibrocystic breast disease

Mechanism of Action: Inhibits output of FSH and LH, reducing ovarian estrogen production

Half life: 4.5 h (variable)

PO: 6–{endash}8 w

Metabolism: Hepatic

Elimination: Renal

Research Notes: Ovulation and cyclic bleeding usually returns 60–{endash}90 d after therapy is discontinued

Adult Dosage: Up to 800 mg/d

Elderly Dosage: Treatment of elderly male patients increases risk of prostatic hypertrophy or prostatic carcinoma

Child Dosage: Not established

Infant Dosage: Not established

Dosage Forms: Capsules: 50 mg, 100 mg, and 200 mg

By System: Endocrine

Warnings: May alter blood glucose levels

Precautions: May cause photosensitivity reactions

Frequent Side Effects: Amenorrhea, decreased breast size, weight gain, irregular menstrual periods

Occasional Side Effects: Edema, muscle cramps, acne, oily skin and hair

Rare Side Effects: Blood in urine, bleeding gums, cataracts, carpal tunnel syndrome, leukocytosis, testicular atrophy, photosensitivity, vaginal burning or itching

Disease States: Cardiac impairment, epilepsy, migraine headache, renal and hepatic impairment, diabetes mellitus, vaginal bleeding

Other Drugs: Anticoagulants, oral antidiabetic agents, insulin, cyclosporine

Lab Tests: Blood pressure, cholic acid concentration, glucose tolerance, HDLs, blood glucose concentration, thyroid function

Administrative Notes: In the treatment of endometriosis and fibrocystic breast disease, it is recommended that therapy begin on the first day of the menstrual cycle after pregnancy has been ruled out

Dantrolene Sodium

Trade Name(s): Dantrium

Chemically Related To: EDTA

Pregnancy Category: Not documented

Medical Category: Malignant hyperthermia therapy; antispastic; Duchenne muscular dystrophy therapy adjunct

Accepted Indications: Malignant hyperthermia, spasticity

Unaccepted Indications: Muscle spasm caused by rheumatic disorders

Mechanism of Action: Interferes with release of Ca2+{plus}, reducing increase in myoplasmic Ca2+{plus} concentration that is associated with malignant hyperthermia and muscle spasms

Half life: PO 9 h; IV, 4 h

PO: 9 h

IV: 5 h

Metabolism: Hepatic

Elimination: Renal

Adult Dosage: 25–{endash}400 mg/d

Child Dosage: Up to 400 mg/d

Infant Dosage: Same as child dose

Dosage Forms: Capsules: 25 mg, 50 mg, and 100 mg; injection: 20 mg

By System: CNS, skeletal

Warnings: May cause drowsiness

Precautions: Avoid alcohol

Frequent Side Effects: Mild diarrhea, dizziness, drowsiness, muscle weakness, nausea and vomiting, extreme tiredness

Occasional Side Effects: Severe diarrhea, respiratory depression, abdominal or stomach cramps, blurred or double vision, chills, fever

Contraindications: Hepatic disease

Antidotal Therapy: May include supportive therapy

Disease States: Cardiac, hepatic and pulmonary function impairment, pre-existing myopathy, neuromuscular disease

Other Drugs: CNS depressants, calcium channel blockers

Lab Tests: Liver function

Administrative Notes: Must be discontinued if symptoms of hepatitis develop during therapy

Daunorubicin Hydrochloride

Trade Name(s): Cerubidine

Pregnancy Category: D

Medical Category: Antineoplastic

Accepted Indications: Acute leukemia, Ewing's sarcoma, neuroblastoma, non-Hodgkin's lymphoma, Wilms' tumor, chronic myelocytic leukemia

Mechanism of Action: Antibacterial/immunosuppressant

Absorption/Distribution: Rapidly distributed, does not cross blood-brain barrier

Half life: 45 min (distribution), 18.5 h (elimination)

Metabolism: Hepatic

Elimination: Biliary

Adult Dosage: Acute lymphocytic leukemia: IV: 45 mg/m2 on d 1–{endash}3 of 32 d course (and possibly d 1–{endash}2 of second course) in combination with vincristine, prednisone, asparaginase, and/or cytarabine. Lifetime maximum of 550 mg/m2.

Elderly Dosage: 60 y and older: IV, 30 mg/m2, as in adult administration

Child Dosage: IV, 25 mg/m2 once/w in combination with vincristine and prednisone

Infant Dosage: Not established

Dosage Forms: Injection: 20 mg

Frequent Side Effects: Stomatitis, leukopenia, esophagitis, infection, nausea, vomiting, hair loss, reddish urine

Occasional Side Effects: Cardiotoxicity in form of CHF, extravasation, hyperuricemia, thrombocytopenia, skin darkening, diarrhea

Rare Side Effects: Pericarditis/myocarditis, allergic reaction

Contraindications: Bone marrow depression, chickenpox, herpes zoster, heart disease

Disease States: Gout, infection, hepatic function impairment

Other Drugs: Probenecid, live virus vaccines, sulfinpyrazone, bone marrow depressants

Lab Tests: Chest x-ray, EKG, platelet count

Deferoxamine Mesylate

Trade Name(s): Desferal

Pregnancy Category: C

Medical Category: Chelating agent

Accepted Indications: Acute iron toxicity, chronic iron toxicity, aluminum toxicity

Unaccepted Indications: Removal of iron deposits from cornea and subconjunctiva

Mechanism of Action: Binds with iron to form ferrioxamine

Absorption/Distribution: PO: poorly absorbed from GI tract; parenteral administration required

Half life: 1 h (distribution), 6 h (elimination)

Metabolism: Unknown

Elimination: Renal, fecal

Adult Dosage: Acute iron toxicity: IM, initially 90 mg/kg, followed by 45 mg/kg up to maximum of 1 g/dose q4–{endash}12h, not to exceed 6 g/d

Elderly Dosage: Use with caution

Child Dosage: Under 3 y: IV, 15 mg/kg/h. 3 y and over: same as adult dose.

Infant Dosage: Under 3 y: IV, 15 mg/kg/h

Dosage Forms: Sterile injection: 500 mg

Warnings: May be stored for only 1 w

Frequent Side Effects: Auditory neurotoxicity, tachycardia, shock, allergic reaction, seizures, flushing, ocular toxicity, pain at site of injection, respiratory distress syndrome

Occasional Side Effects: Diarrhea, difficult urination, fever, hypocalcemia, leg cramps, thrombocytopenia, urine color change

Contraindications: Anuria, renal disease, oliguria

Other Drugs: Ascorbic acid, epoetin

Lab Tests: Total iron-binding capacity, ferritin concentrations

Demeclocycline Hydrochloride

Trade Name(s): Declomycin

Chemically Related To: Tetracycline

Pregnancy Category: D

Medical Category: Antibacterial, diuretic

Accepted Indications: Acne, actinomycosis, anthrax, bronchitis, brucellosis, conjunctivitis, GI infections, psittacosis, Q fever, typhus

Mechanism of Action: Inhibits cell protein synthesis

Absorption/Distribution: 66% absorbed

Half life: 10–{endash}17 h

PO: 2–{endash}4 h

Metabolism: Hepatic

Elimination: Renal, fecal

Research Notes: Onset of action in SIADH, 24–{endash}48 h

Adult Dosage: 150 mg q.i.d. up to 2.4 g/d

Elderly Dosage: No specific information known

Child Dosage: Up to 8 y: not recommended because may cause permanent discoloration of teeth; 8 y and over: 1.65–{endash}3.3 mg/kg q.i.d.

Infant Dosage: Not recommended because may cause permanent discoloration of teeth

Dosage Forms: Capsules: 150 mg; tablets: 150 mg and 300 mg

By System: Release of ADH

Warnings: May cause photosensitivity; may interfere with oral contraception

Precautions: Take entire prescription even if symptoms disappear

Frequent Side Effects: Discoloration of children's teeth, photosensitivity, CNS toxicity

Occasional Side Effects: Nephrogenic diabetes insipidus, discolored tongue

Rare Side Effects: Liver problems, pancreatitis

Disease States: Kidney or liver problems, nephrogenic diabetes insipidus

Nutrition: Do not take within 3 h after consumption of milk and other dairy products

Other Drugs: Antacids, calcium supplements, cholestyramine, penicillins, estrogen–{endash}containing contraceptives, vitamin A

Lab Tests: BUN, bilirubin, catecholamines

Deserpidine/Methyclothiazide

Trade Name(s): Enduronyl

Pregnancy Category: C

Medical Category: Antihypertensive

Accepted Indications: Hypertension

Adult Dosage: ½–{endash}1 tablet/d as determined by individual titration

Child Dosage: Not established

Dosage Forms: Tablets: 0.25 mg/5 mg and 0.5 mg/5 mg

Warnings: Elderly may be more sensitive to drug's effects

Desipramine Hydrochloride

Trade Name(s): Norpramin

Chemically Related To: Tricyclic depressants

Pregnancy Category: C

Medical Category: Antidepressant

Accepted Indications: Mental depression; anxiety, neurogenic pain; attention deficit disorder; narcolepsy; bulimia; cocaine withdrawal

Mechanism of Action: Predominantly inhibits the reuptake of norepinephrine

Absorption/Distribution: Rapidly absorbed

Half life: 12–{endash}24 h

Peak activity: Onset of action, 2-3 w

Metabolism: Hepatic

Elimination: Renal over several days

Research Notes: Not dialyzable

Adult Dosage: 100–{endash}300 mg/d

Elderly Dosage: Up to 150 mg/d

Child Dosage: 6–{endash}12 y: 1–{endash}5 mg/kg, adolescents: 25-100 mg/d

Dosage Forms: Tablets:10 mg, 25 mg, 50 mg, 75 mg, 100 mg, and 150 mg

By System: CNS

Precautions: Children are more sensitive to acute overdosage (potentially fatal) than adults

Frequent Side Effects: Anticholinergic effects, nausea, weight gain, dizziness

Occasional Side Effects: Diarrhea, excessive sweating, heartburn, arrhythmia, nervousness

Rare Side Effects: Agranulocytosis, alopecia, anxiety, cholestatic jaundice, galactorrhea, seizures, SIADH, tinnitus

Overdosage: Confusion, convulsions, drowsiness, enlarged pupils, tachycardia or bradycardia, fever, hallucinations, vomiting

Disease States: Alcoholism, asthma, bipolar disorder, blood disorders, cardiovascular disorders, GI disorders, glaucoma, hepatic or renal function impairment, hyperthyroidism, schizophrenia, seizure disorders, urinary retention

Other Drugs: Alcohol, CNS depressants, antithyroid agents, cimetidine, clonidine, guanadrel, guanethidine, phenothiazines, metrizamide, MAO inhibitors, sympathomimetics

Lab Tests: Metyrapone test

Administrative Notes: May cause photosensitivity; avoid alcoholic beverages

Desmopressin Acetate

Trade Name(s): DDAVP, Stimate

Chemically Related To: Biogenic peptide

Pregnancy Category: B

Medical Category: Antidiuretic (central diabetes insipidus, primary nocturnal enuresis), antihemorrhagic

Accepted Indications: Central diabetes insipidus, primary nocturnal enuresis, hemophilia A, von Willebrand's disease

Mechanism of Action: Increases permeability of renal tubular epithelium to water

Absorption/Distribution: Less than 20% absorbed from nasal mucosa

Half life: Fast phase, 7.8 min; slow phase, 75.5 min

Peak activity: Intranasal 1–{endash}5 h

Metabolism: Renal

Elimination: Renal

Research Notes: Onset of action as an antihemorrhagic is within several min, 15–{endash}30 min for von Willebrand factor levels, if given IV

Adult Dosage: Maintenance: 10–{endash}40 m{mu}g/d

Elderly Dosage: Restrict of fluid intake

Child Dosage: 3 m–{endash}12 y: maintenance: 2–{endash}4 m{mu}g/kg/d

Infant Dosage: Up to 3 m: not established

Dosage Forms: Nasal solution: 10 and 100 m{mu}g, injection: 4 m{mu}g/mL

By System: Cardiovascular

Occasional Side Effects: Abdominal cramps, headache, nausea

Rare Side Effects: Pain in vulva, hypertension, water intoxication

Antidotal Therapy: May include reduction of dosage, furosemide

Disease States: Allergic rhinitis, nasal congestion, coronary artery disease

Other Drugs: Lithium, norepinephrine, clofibrate, carbamazepine, demeclocycline

Administrative Notes: Refrigerate nasal solution

Desonide

Trade Name(s): Desowen, Tridesilon

Chemically Related To: Corticosteroids

Pregnancy Category: C

Medical Category: Steroidal anti-inflammatory

Accepted Indications: Skin disorders, contact dermatitis, eczema, pruritus, psoriasis, xerosis

Unaccepted Indications: Acne

Mechanism of Action: Augments synthesis of inhibitory enzymes responsible for anti-inflammatory action

Absorption/Distribution: Absorbed systemically and transdermally

Metabolism: Hepatic

Elimination: Renal

Adult Dosage: Topical to skin b.i.d. to q.i.d.

Elderly Dosage: Watch frequency because of skin atrophy

Child Dosage: Topical to skin once daily

Infant Dosage: Same as child dose

Dosage Forms: Cream: 0.05%; ointment: 0.05%

By System: Dermal

Warnings: For external use only; do not use in and around the eyes

Precautions: Do not bandage the treated skin area

Occasional Side Effects: Burning sensation, dryness, irritation, itching, rash

Rare Side Effects: Acneiform eruptions, cataracts, Cushing's syndrome, hirsutism, contact dermatitis, numbness in fingers

Disease States: Infection, pre-existing skin atrophy, cataracts, diabetes mellitus, glaucoma, tuberculosis

Lab Tests: Glucose, total eosinophil count, corticotropin test

Desoxyribonuclease

Trade Name(s): Not available a a single agent

Chemically Related To: Nucleic acids; proteolytic enzyme extracted from bovine pancreas

Medical Category: Skin and mucous membrane agent; debridement agent

Accepted Indications: Skin lesions, wounds, vaginitis, irrigating agent

Mechanism of Action: Attacks DNA in blood clots and fibrinous wound exudate

Desoxyribonuclease/Fibrinolysin

Trade Name(s): Elase

Medical Category: Topical debridement enzyme

Accepted Indications: Debridement of surgical wounds, ulcerative lesions, second- and third-degree burns, circumcision episiotomy; cervicitis and vaginitis; infected wounds, otorhinolaryngologic wounds, superficial hematomas

Adult Dosage: Adjusted on individual basis

Elderly Dosage: Adjusted on individual basis

Child Dosage: Adjusted on individual basis

Infant Dosage: Adjusted on individual basis

Dosage Forms: Ointment: 666.6 units/1 unit/g; lyophilized powder: 15,000 units/25 units/30 mL vial

By System: Dermal

Dexamethasone

Trade Name(s): Aeroseb-Dex, A/K-Dex, Baldex, Decaderm, Decadron, Decaspray, Dexair, I-Methasone, Maxidex, Ocu-Dex

Chemically Related To: Beclomethasone

Pregnancy Category: C

Medical Category: Corticosteroid, inhalation anti-inflammatory, nasal steroidal anti-inflammatory, ophthalmic steroidal anti-inflammatory; otic steroidal anti-inflammatory, topical steroidal anti-inflammatory

Accepted Indications: Psoriasis, eczema, xerosis, mild to moderate atopic dermatitis, intertrigo, lichen planus, contact dermatitis, ophthalmic disorders, chronic bronchial asthma, rhinitis, nasal allergic disorders, nasal inflammatory conditions, nasal polyps, otitis externa, infective otitis, polymorphous light eruption, pruritus

Unaccepted Indications: Acne, gingivitis, acute bronchospasm, non-asthmatic bronchitis, degenerative ocular disorders

Mechanism of Action: Stimulates synthesis of DNA and inhibitory enzymes that stabilize cell membranes responsible for inflammation

Absorption/Distribution: Rapidly and extensively absorbed from nasal mucosa; readily absorbed from GI mucosa; absorbed into aqueous humor, cornea, iris, choroid ciliary body, and retina; absorbed systemically across the stratum corneum

Half life: 190 min

Peak activity: 1–{endash}2 h

Metabolism: Hepatic

Elimination: Renal

Adult Dosage: Nasal aerosol: initially 200 m{mu}g in each nostril b.i.d. or t.i.d., dosage decreased according to response; ophthalmic suspension: topical, to the conjunctiva, 1–{endash}2 drops 4–{endash}6 times/d; sodium phosphate ophthalmic ointment: topical, to the conjunctiva, a thin strip t.i.d. or q.i.d.; sodium phosphate ophthalmic solution: topical, to the conjunctiva, 1–{endash}2 drops up to 6 times/d; topical, to the skin, t.i.d. or q.i.d.; topical aerosol: topical, to the skin, b.i.d. to q.i.d.; cream: topical, to the skin, t.i.d. to q.i.d.; tablets: 500 m{mu}g–{endash}9 mg/d

Elderly Dosage: Reduce dosage because of pre-existing skin atrophy; ophthalmic suspension, sodium phosphate ophthalmic ointment and sodium phosphate ophthalmic solution: same as adult dose

Child Dosage: Nasal aerosol: under 6 y: not recommended; 6–{endash}12 y: 100–{endash}200 m{mu}g in each nostril b.i.d.; ophthalmic suspension, sodium phosphate ophthalmic ointment and sodium phosphate ophthalmic solution: same as adult dose; gel: topical to the skin 0.1% once daily or b.i.d.; topical aerosol: topical, to the skin, 0.01% or 0.04% once daily or b.i.d.; cream: topical to the skin, once daily

Infant Dosage: Same as child dose

Dosage Forms: Gel: 0.1%; aerosol: 0.01% and 0.04%; inhalation aerosol: 100 m{mu}g/metered spray; sodium phosphate nasal aerosol: 100 m{mu}g/metered spray; ophthalmic suspension: 0.1%; sodium phosphate ophthalmic ointment: 0.05%; sodium phosphate ophthalmic solution: 0.1%; cream: 0.1%

By System: Dermal, respiratory

Warnings: Topical forms for external use only

Precautions: If symptoms do not improve within 1 w or become worse, contact physician; do not bandage or otherwise wrap skin areas treated with topical forms

Frequent Side Effects: Cough, dry mouth, dysphonia, throat irritation, blurred vision

Occasional Side Effects: Contact dermatitis, numbness in fingers, purpura, skin atrophy, oropharyngeal candidiasis, dry throat, headache, nausea, skin bruising, unpleasant taste, crusting inside nose, sore throat, sores inside nose, allergic reaction, sneezing, corneal thinning, secondary ocular infection, burning or stinging of eyes or ears, secondary skin infection

Rare Side Effects: Acneiform eruptions, cataracts, Cushing's syndrome, glaucoma, hirsutism, increased bronchospasm, esophageal candidiasis, nasal candidiasis, nasal septal perforation, ocular hypertension, menstrual changes, perioral dermatitis, ecchymosis, edema, gastric ulcer, hypertension, hypopigmentation, skin maceration, unusual scalp hair loss

Contraindications: Diabetes, systemic infections

Antidotal Therapy: May include proper withdrawal and dosage decreasing methods

Disease States: Infection at treatment site, pre-existing skin atrophy, cataracts, glaucoma, tuberculosis, osteoporosis, ocular herpes simplex, ocular fungal diseases, herpes simplex keratitis, acute viral disease, aural fungal diseases, chronic otitis media, perforation of eardrum membrane, acute ear infection

Other Drugs: Antiglaucoma agents, anticholinergics, contact lenses

Lab Tests: Glucose, total eosinophil count, adrenal function as assessed by corticotropin, nitroblue tetrazolium test for bacterial infection, hypothalamic-pituitary-adrenal axis function

Dexamethasone Sodium Phosphate

Trade Name(s): AK-Dex, Baldex, Decadron, Maxidex, OcuDex

Chemically Related To: Corticosteroids

Pregnancy Category: C

Medical Category: Adrenocorticoid (ophthalmic); anti-inflammatory (steroidal), ophthalmic

Accepted Indications: Treatment of ophthalmic disorders

Unaccepted Indications: Degenerative ocular disorders

Mechanism of Action: Inhibits mediators of inflammation

Absorption/Distribution: Absorbed into aqueous humor, cornea, iris, ciliary body, and retina. Some small systemic absorption can occur

Research Notes: Long-term therapy should be avoided

Adult Dosage: Topical to conjunctiva t.i.d. or q.i.d.

Elderly Dosage: See adult dose

Child Dosage: See adult dose

Infant Dosage: Use with caution in children under 2 y

Dosage Forms: Ophthalmic ointment .05%, ophthalmic solution .1%

By System: Ocular

Warnings: For the eye; do not contaminate applicator tip

Precautions: Have ophthalmological examinations during long-term therapy

Frequent Side Effects: Mild blurred vision

Occasional Side Effects: Optic nerve damage, ocular hypertension, corneal thinning, secondary ocular infection

Rare Side Effects: Burning, redness, or watering of eyes

Contraindications: Ocular fungal disorders, herpes simplex, ocular TB, acute viral disease

Antidotal Therapy: May include dilution with fluids

Disease States: Cataracts, diabetes mellitus, thinning of cornea, infections of cornea, chronic glaucoma

Other Drugs: Antiglaucoma agents, anticholinergics, contact lenses

Administrative Notes: Dispense in original unopened container

Dexamethasone Sodium Phosphate/Neomycin Sulfate (Ophthalmic)

Trade Name(s): Ak-Neo-Dex, Neodecadron, Neo-Dex, Neo Dexair

Medical Category: Topical anti-infective

Accepted Indications: Inflammatory ocular conditions; conjunctivitis; chronic anterior uveitis and corneal injury from chemical, radiation, or thermal burns or from penetration by foreign bodies

Adult Dosage: Ointment: thin coating in eye t.i.d.–{endash}q.i.d.; solution: initial dose, 1–{endash}2 drops in eye/h during day and q2h at night, reduce to 1 drop q4h

Dosage Forms: Ophthalmic solution: 1 mg/3.5 mg/mL; ophthalmic ointment: 0.05 mg/3.5 mg/g

Dexamethasone/Neomycin Sulfate/Polymyxin B Sulfate

Trade Name(s): Ak-Trol, Dexacidin, Dex-Ide, Dexamycin, Dexasporin, Maxitrol, Ocu-Trol

Pregnancy Category: Adequate studies have not been done

Medical Category: Topical anti-infective

Accepted Indications: Inflammatory ocular conditions; conjunctivitis; chronic anterior uveitis and corneal injury from chemical, radiation, or thermal burns or from penetration by foreign bodies

Adult Dosage: Suspension: 1–{endash}2 drops in conjunctival sac q3–{endash}4h; ointment: small amount in conjunctival sac q3–{endash}4h

Dosage Forms: Ophthalmic ointment: 0.1%/0.35%/10,000 units/g; ophthalmic suspension: 0.1%/0.35%/10,000 units/mL

Dexamethasone/Tobramycin

Trade Name(s): Tobradex

Medical Category: Topical anti-infective

Accepted Indications: Inflammatory ocular conditions; conjunctivitis; chronic anterior uveitis and corneal injury from chemical, radiation, or thermal burns or from penetration by foreign bodies

Adult Dosage: Suspension: 1–{endash}2 drops q4–{endash}6h; ointment: small amount up to t.i.d.–{endash}q.i.d.

Child Dosage: Safety and effectiveness not established

Dosage Forms: Ointment: 0.1%/0.3%; suspension: 0.1%/0.3%

Dexchlorpheniramine Maleate

Trade Name(s): Dexchlor, Poladex, Polaramine, Polaramine Repetabs

Chemically Related To: Diphenhydramine

Pregnancy Category: B

Medical Category: Antihistaminic (H1-receptor)

Accepted Indications: Rhinitis, conjunctivitis, pruritus, urticaria, angioedema, urticarial transfusion reactions, sneezing, rhinorrhea

Mechanism of Action: Competes with histamine for receptor site

Absorption/Distribution: Well absorbed

Half life: 20 h

PO: 4–{endash}8 h

Metabolism: Hepatic

Elimination: Renal

Adult Dosage: 2–{endash}24 mg/d

Elderly Dosage: May be more sensitive to the effects of usual adult dosage

Child Dosage: 2–{endash}4 mg/d

Dosage Forms: Tablets: 2 mg; syrup: 2 mg/5 mL; extended-release tablets: 4 mg and 6 mg

By System: Respiratory

Warnings: May cause drowsiness; avoid alcohol

Precautions: May mask ototoxic effects of large doses of salicylates; dry mouth possible

Frequent Side Effects: Drowsiness, thickening of mucus

Occasional Side Effects: Blood dyscrasias, cardiac arrhythmias

Rare Side Effects: Blurred vision, confusion, difficulty in urination, dizziness, dry mouth, tachycardia, increased sweating, loss of appetite, photosensitivity, tinnitus, rash

Contraindications: Impairment of hepatic function

Overdosage: Anticholinergic effects, cardiac arrhythmias, hallucinations

Antidotal Therapy: May include symptomatic and supportive treatment

Disease States: Urinary retention, bladder neck obstruction, glaucoma, prostatic hypertrophy

Other Drugs: CNS depressants, anticholinergics, erythromycin, MAO inhibitors, ototoxic medications, photosensitizing medication

Lab Tests: Skin tests with allergen extracts

Dexchlorpheniramine/Guaifenesin/Pseudoephedrine

Trade Name(s): Polaramine Expectorant

Pregnancy Category: C

Medical Category: Antihistamine, decongestant, expectorant

Accepted Indications: Allergies, colds

Adult Dosage: 5–{endash}10 mL q6–{endash}8h

Child Dosage: 2–{endash}6 y: 1.25–{endash}2.5 mL; 6–{endash}12 y: 2.5–{endash}5 mL q6–{endash}8h

Dosage Forms: Oral solution: 2 mg/100 mg/20 mg

Dextran

Trade Name(s): Dextran 40, Dextran 70, Dextran 75

Chemically Related To: Glucose

Pregnancy Category: C

Medical Category: Fluid replacement preparation

Accepted Indications: Early fluid replacement, plasma volume expander, venous thrombosis (prophylaxis), pulmonary embolism, poor circulation

Mechanism of Action: Expands plasma volume, provides fluid replacement

Elimination: Renal, fecal

Research Notes: Use of dextran sulfate sodium in treatment of AIDS is under sponsor Ueno Fine Chemicals Industry, Ltd., of Japan

Adult Dosage: Dextran 40: 10 mL/kg initially, up to 20 mL/kg in first 24 h; Dextran 70 and 75: 500–{endash}1000 mL IV, not to exceed 20 mL/kg in first 24 h

Child Dosage: Do not exceed 20 mL/kg (total dosage)

Dosage Forms: Dextran 40: parenteral injection for IV 10%; Dextran 70: parenteral injection for IV 6%; Dextran 75: parenteral injection for IV 6%

Warnings: Assess hydration before beginning therapy

Precautions: Monitor urine flow; check hemoglobin and hematocrit

Side/Adverse Effects: Nausea/vomiting, urticaria, fever, nasal congestion, anaphylaxis, wheezing, tightness in the chest, mild hypotension

Contraindications: Pulmonary edema, kidney problems, extreme dehydration

Disease States: Hemorrhage, heart problems

Lab Tests: Blood glucose determinations, tests with turbidimetric measurements

Administrative Notes: These compounds do not contain preservatives; therefore, partially used containers should be discarded

Dextroamphetamine Sulfate

Trade Name(s): Dexedrine

Scheduled Class: II

Pregnancy Category: C

Accepted Indications: Narcolepsy, attention deficit disorder (ADD)

Unaccepted Indications: Appetite suppressants, fatigue, rest replacement

Mechanism of Action: Increased motor activity and alertness

Half life: 10–{endash}12 h

Metabolism: Hepatic

Elimination: Renal

Adult Dosage: 5–{endash}60 mg once daily or in divided doses

Elderly Dosage: Same as adult dose

Child Dosage: ADD: under 3 y: not recommended; 3–{endash}6 y: 2.5 mg once daily, dose increased as needed; 6 y and over: 5 mg once daily, dose increased as needed. Narcolepsy: under 3 y: not recommended; 3–{endash}6 y: not established; 6–{endash}12 y: 5 mg once daily, dose increased as needed; 12 y and over: 10 mg once daily, dose increased as needed

Infant Dosage: Not recommended

Dosage Forms: Capsules: 5 mg, 10 mg, and 15 mg; tablets: 5 mg and 10 mg

Frequent Side Effects: CNS stimulation, arrhythmia, irritability, nervousness

Occasional Side Effects: Blurred vision, dizziness, diarrhea, constipation, anorexia, stomach cramps, nausea, headache, dry mouth, increased sweating, unpleasant taste

Rare Side Effects: Chest pain, Tourette's syndrome, changes in libido, tachycardia, hyperthermia

Contraindications: Arteriosclerosis, glaucoma, hypertension, drug abuse, Tourette's syndrome

Antidotal Therapy: May include emesis, gastric lavage, IV fluids

Disease States: Agitation, cardiovascular disease, hyperthyroidism

Other Drugs: Acidifiers, meperidine, MAO inhibitors, beta-blockers, CNS stimulants, thyroid hormones, tricyclic antidepressants, digitalis glycosides

Lab Tests: Urinary steroid determinations

Dextromethorphan Hydrobromide

Trade Name(s): Benylin DM, Children's Hold, Creo-Terpin, Drixoral Cough Liquid Tablets, Hold, Pertussin CS, Pertussin ES, Robitussin Cough Calmers, Robitussin Pediatric, Sucrets Cough Control, Vicks Formula 44-Pediatric

Chemically Related To: Levorphanol

Pregnancy Category: Problems in humans not documented

Medical Category: Antitussive

Accepted Indications: Cough

Unaccepted Indications: Chronic cough associated with smoking, emphysema, or asthma

Mechanism of Action: Acts on cough center in medulla oblongata

Absorption/Distribution: Rapidly absorbed

Metabolism: Hepatic

Elimination: Renal

Research Notes: Onset of action usually within 0.5 h; duration of action, up to 6 hours

Adult Dosage: 10–{endash}20 mg/4 h to 120 mg/d

Elderly Dosage: Same as adult dose

Child Dosage: 2–{endash}6 y: 2.5–{endash}5 mg/4 h, not to exceed 30 mg/d; 6-12 y: 5–{endash}10 mg/4 h, not to exceed 60 mg/d

Infant Dosage: Up to 2 y: not recommended

Dosage Forms: Lozenges: 5 mg and 7.5 mg; syrup: USP 3.5 mg/5 mL, 7.5 mg/5 mL, 10 mg/5 mL, 15 mg/5 mL; chewable tablets: 15 mg; capsules: 30 mg

By System: Respiratory

Warnings: Chew chewable tablets well before swallowing

Precautions: Check with physician if cough continues for more than 7 d

Occasional Side Effects: Dizziness, drowsiness, GI upset

Overdosage: Confusion, drowsiness, nausea/vomiting, excitement, nervousness, irritability

Antidotal Therapy: May include naloxone HCl, supportive measures

Disease States: Asthma, liver problems, atopy (in children)

Other Drugs: CNS depressants, MAO inhibitors, penicillins, tetracyclines, salicylates, phenobarbital

Dextromethorphan Hydrobromide/Iodinated Glycerol

Trade Name(s): Iodur DM, Iophen DM, Tusso-DM

Pregnancy Category: X

Medical Category: Antitussive, expectorant

Adult Dosage: 5–{endash}10 mL q4h

Child Dosage: 2–{endash}6 y: 1.25–{endash}2.5 mL; 6–{endash}12 y: 2.5–{endash}5 mL q4h

Dosage Forms: Liquid: 10 mg/30 mg/5 mL; oral solution: 10 mg/30 mg/5 mL

Dextromethorphan Hydrobromide/Promethazine Hydrochloride

Trade Name(s): Phenameth DM, Phenergan with Dextromethorphan, Pherazine DM, Prometh with Dextromethorphan, Promethazine DM

Pregnancy Category: C

Medical Category: Antitussive, antihistamine

Accepted Indications: Cough and cold

Adult Dosage: 5 mL q4–{endash}6h up to 30 mL/d

Child Dosage: 2–{endash}6 y: 1.25–{endash}2.5 mL q4–{endash}6h up to 10 mL/d; 6–{endash}12 y: 2.5–{endash}5 mL q4–{endash}6h up to 20 mL/d

Dosage Forms: Syrup: 15 mg/6.25 mg/5 mL

Dezocine

Trade Name(s): Dalgan

Chemically Related To: Opioids

Pregnancy Category: C

Medical Category: Analgesic

Accepted Indications: Short-term pain

Unaccepted Indications: Chronic pain

Mechanism of Action: Opioid agonist/antagonist

Absorption/Distribution: Rapid and complete

Half life: IM: 2.2 h (elimination); IV: 1.7–{endash}2.8 h (elimination)

Peak activity: 1–{endash}2 h

IM: 10–{endash}90 min

Metabolism: Hepatic

Elimination: Renal

Adult Dosage: IM: 5–{endash}20 mg q3–{endash}6h; IV: 2.5–{endash}10 mg q2–{endash}4h

Elderly Dosage: Same as adult dose

Child Dosage: Up to 18 y: not established

Infant Dosage: Not established

Dosage Forms: Injection: 5 mg/mL, 10 mg/mL, and 15 mg/mL

Warnings: Avoid alcohol

Frequent Side Effects: Drowsiness, GI upset

Occasional Side Effects: CNS effects, flushing or redness of skin

Rare Side Effects: Difficult or decreased urination, arrhythmia, respiratory depression, chest pain, edema, hypertension, hypotension, thrombophlebitis, atelectasis, CNS toxicity

Contraindications: Asthma, respiratory disease, opioid dependence

Overdosage: Cold, clammy skin; severe dizziness; confusion, nervousness, restlessness, convulsions, drowsiness, hypotension, pinpoint pupils, troubled breathing, and weakness; bradycardia; unconsciousness

Antidotal Therapy: May include 0.4–{endash}2 mg naloxone, IV fluids

Disease States: Cardiovascular disease, emotional instability, recent GI surgery, head injury, liver and renal function impairment

Other Drugs: CNS depressants, naltrexone, opioid analgesics, monoamine oxidase inhibitor

Administrative Notes: May be habit forming

Diazepam

Trade Name(s): T-Quil, Valium, Vazepam

Chemically Related To: Benzodiazepines

Scheduled Class: IV

Abuse Potential: Mild

Pregnancy Category: C

Medical Category: Antianxiety agent, sedative-hypnotic, amnestic, anticonvulsant, skeletal muscle relaxant adjunct

Accepted Indications: Anxiety

Mechanism of Action: Depresses CNS at limbic and other levels of brain

Absorption/Distribution: Rapidly absorbed

Half life: 20–{endash}70 h

PO: 0.5–{endash}2 h

IM: 0.5–{endash}1.5 h

IV: Within 0.25 h

Metabolism: Hepatic

Elimination: Renal

Research Notes: Preanesthetic administration can impair recent memory

Adult Dosage: Oral solution: 2–{endash}10 mg b.i.d. to q.i.d.

Elderly Dosage: 2–{endash}2.5 mg once daily or b.i.d.

Child Dosage: 6 m and over: 1–{endash}2.5 mg t.i.d. or q.i.d.

Infant Dosage: Up to 6 m: not recommended

Dosage Forms: Extended-release capsules: 15 mg; oral solution: 5 mg/mL, 5 mg/5 mL; tablets: 2 mg, 5 mg, 10 mg; injection: 5 mg/mL; sterile emulsion; rectal solution

By System: CNS, subcortical nuclei

Warnings: May cause drowsiness; avoid alcohol

Frequent Side Effects: Clumsiness, dizziness, drowsiness, slurred speech, irritability, insomnia

Occasional Side Effects: Abdominal cramps, diarrhea, headache, trembling, tachycardia

Rare Side Effects: Blood dyscrasias, liver problems, seizures, hallucinations, withdrawal symptoms

Overdosage: Confusion, decreased reflexes, drowsiness, bradycardia, respiratory problems, slurred speech, staggering

Antidotal Therapy: May include emesis/gastric lavage, activated charcoal, oxygen and IV fluids, IV vasopressor, flumazenil

Disease States: Acute alcohol intoxication, coma, shock, convulsions, glaucoma, liver problems, mental depression, myasthenia gravis

Other Drugs: Erythromycin, antihypertensives, CNS depressants, zidovudine, levodopa, estrogen–{endash}containing contraceptives

Lab Tests: Metyrapone, sodium iodide

Administrative Notes: If IM injection used, penetrate deep into deltoid muscle

Diazoxide

Trade Name(s): Proglycem, Hyperstat

Chemically Related To: Thiazides

Pregnancy Category: C

Medical Category: Antihypoglycemic, antihypertensive

Accepted Indications: (Oral) hypoglycemia, (IV) hypertension

Unaccepted Indications: Chronic hypertension, functional hypoglycemia

Mechanism of Action: Inhibition of insulin release, arteriolar vasodilatation and decreased peripheral resistance

Absorption/Distribution: Rapidly absorbed; high protein binding

Half life: 20–{endash}36 h

PO: 1 h

IV: 2–{endash}5 min

Metabolism: Hepatic

Elimination: Renal; 50% unchanged

Research Notes: PO: onset of action 1 h; duration of action 8 h IV: onset of action 1 min; duration of action 2–{endash}12 h

Adult Dosage: Capsules and suspension: 1 mg/kg t.i.d., initially; 3–{endash}8 mg/kg/d, maintenance; injection: IV up to 150 mg, repeated every 5–{endash}15 min if necessary, up to 1.2 g/d

Elderly Dosage: Same as adult dose

Child Dosage: Capsules and oral suspension: same as adult dose; injection: 1–{endash}3 mg/kg, repeated in 5–{endash}15 min if necessary

Infant Dosage: Capsules and oral suspension, initial: 3.3 mg/kg t.i.d.; maintenance: 8–{endash}15 mg/kg/d

Dosage Forms: Capsules: 50 mg; oral suspension: 50 mg/mL, injection: 15 mg/mL

Precautions: Protect oral suspension and injection from freezing and from light, shake oral suspension well

Frequent Side Effects: Edema

Occasional Side Effects: Tachycardia, hyperglycemia, changes in ability to taste, ileus, loss of appetite, nausea, stomach pain, vomiting

Rare Side Effects: Allergic reaction, angina pectoris, ischemia, myocardial infarction, transient focal cerebral ischemic attacks, thrombocytopenia

Contraindications: Acute aortic dissection, coronary or cerebral insufficiency

Overdosage: Hyperglycemia, ketoacidosis

Antidotal Therapy: May include insulin, fluids, patient monitoring

Disease States: Gout, hypokalemia, renal function impairment, compensatory hypertension, inadequate cardiac reserve

Other Drugs: Hydantoin anticonvulsants, vasodilators, hypotension–{endash}producing medications

Lab Tests: Uric acid, hematocrit, glucose, BUN

Administrative Notes: Extrapyramidal effects and hypertrichosis may appear with long-term use

Dibucaine

Trade Name(s): Nupercainal

Pregnancy Category: Studies in humans have not been done

Medical Category: Local anesthetic, mucosal-local anesthetic

Accepted Indications: Minor skin disorders, anorectal disorders

Mechanism of Action: Blocks the initiation and conduction of nerve impulses

Absorption/Distribution: Readily absorbed through mucous membranes

Metabolism: Hepatic, renal

Elimination: Renal

Research Notes: Onset of action up to 15 min, duration of action 2–{endash}4 h

Adult Dosage: Topical, to the skin, t.i.d. or q.i.d.

Elderly Dosage: Same as adult dose

Child Dosage: Same as adult dose

Infant Dosage: Dosage must be individualized

Dosage Forms: Cream: 0.5%. Ointment: 1%.

Occasional Side Effects: Angioedema, dermatitis

Rare Side Effects: CNS depression, methemoglobinemia

Contraindications: Local infection, severe skin disorders

Antidotal Therapy: May include vasopressor, IV fluids

Dichloralphenazone

Trade Name(s): Not available as a single agent

Medical Category: Sedative, hypnotic

Mechanism of Action: Reduces emotional reaction to pain

Metabolism: Hepatic, renal

Elimination: Renal

Research Notes: A complex of chloral hydrate and antipyrine

By System: CNS

Dichlorphenamide

Trade Name(s): Daranide

Chemically Related To: Acetazolamide

Pregnancy Category: Problems not documented

Medical Category: Antiglaucoma agent

Accepted Indications: Glaucoma

Mechanism of Action: Carbonic anhydrase inhibitor. Decreases production of aqueous humor by decreasing bicarbonate ion concentration

Absorption/Distribution: Well absorbed

PO: 2–{endash}4 h

Research Notes: Onset of action, 0.5–{endash}1 h; duration of action, 6–{endash}12 h

Adult Dosage: Initial dose: 100–{endash}200 mg; maintenance: 25–{endash}50 mg 1–{endash}3 times daily

Elderly Dosage: Kidney problems may necessitate a reduction in dosage

Child Dosage: Not established

Infant Dosage: Not established

Dosage Forms: Tablets: 50 mg

By System: Aqueous humor

Warnings: May cause drowsiness or hypokalemia

Frequent Side Effects: Tiredness; diarrhea; increase in urination; loss of appetite; metallic taste; weight loss

Occasional Side Effects: Crystalluria, depression, dizziness

Rare Side Effects: Acidosis, blood dyscrasias, confusion, seizures, constipation, headache

Disease States: Adrenal gland failure, diabetes mellitus, respiratory acidosis, liver or kidney problems

Other Drugs: Quinidine, antidiabetic agents, anticholinergics, digitalis, diuretics

Lab Tests: Urine protein, blood glucose, serum potassium, plasma bicarbonate

Administrative Notes: If potassium supplement is required, dispense a supplement that does not contain chloride. Need ample fluid intake to prevent kidney stones; take with meals or food to lessen GI upset.

Diclofenac

Trade Name(s): Cataflam, Voltaren

Chemically Related To: Similar to aspirin

Pregnancy Category: B

Medical Category: Anti-inflammatory, analgesic, nonsteroidal

Accepted Indications: Rheumatic inflammations; bursitis and other nonrheumatic inflammations

Mechanism of Action: Decreases peripheral inflammatory mechanisms through prostaglandin inhibition

Absorption/Distribution: Well absorbed

Half life: Up to 6 h

Peak activity: 3 h

PO: 3 h

Metabolism: Hepatic

Elimination: Renal

Adult Dosage: 25–{endash}150 mg/d

Child Dosage: 2 mg/kg/d

Dosage Forms: Tablets: 25 mg, 50 mg, and 75 mg

By System: Anti-inflammatory analgesic (nonsteroidal) systemic

Warnings: May cause bronchoconstriction; elderly patients may require decreased dosage

Precautions: Caution in patients who must restrict sodium intake

Frequent Side Effects: Increased blood pressure, headache, weight gain, constipation, stomach cramps

Occasional Side Effects: GI bleeding; bloating; chest pain associated with angina; arrhythmia

Rare Side Effects: Bloody or cloudy urine, blurred vision, decreased hearing, altered liver function tests, renal impairment

Overdosage: GI distress, renal failure

Antidotal Therapy: May include emesis or gastric lavage, activated charcoal

Disease States: Blood dyscrasias; bone marrow depression; symptoms of nasal polyps

Other Drugs: Acetaminophen, adrenocorticoids, antidiabetics

Lab Tests: Liver function, serum uric acid concentrations

Dicloxacillin Sodium

Trade Name(s): Dycill, Dynapen, Pathocil

Chemically Related To: Penicillin

Pregnancy Category: B

Medical Category: Antibacterial

Accepted Indications: Pneumonia (staphylococcal), sinusitis, skin and soft tissue infections, biliary tract infections

Unaccepted Indications: Meningitis

Mechanism of Action: Bactericidal; inhibits bacterial cell wall synthesis

Absorption/Distribution: 37%–{endash}50% oral absorption, decreased by food; very high protein binding

Half life: 0.5–{endash}1 h

PO: 0.5–{endash}1 h

Metabolism: Hepatic

Elimination: Renal

Research Notes: Penicillinase-resistant penicillin

Adult Dosage: 1–{endash}6 g/d

Child Dosage: Up to 40 kg: 3.125–{endash}6.25 mg/kg/d; 40 kg and over: same as adult dosage

Infant Dosage: Neonates: not established; infants up to 40 kg: 3.125–{endash}6.25 mg/kg/d

Dosage Forms: Tablets: 125 mg, 250 mg, and 500 mg

Warnings: Do not take unprescribed antidiarrheals

Frequent Side Effects: GI reactions, oral candidiasis

Rare Side Effects: Unusual bleeding

Antidotal Therapy: No specific antidote

Disease States: Asthma, eczema, seasonal allergic rhinitis, hives, GI disease, infectious mononucleosis, kidney problems

Other Drugs: Anticoagulants, thrombolytic agents, potassium supplements, tetracyclines, estrogen–{endash}containing contraceptives, probenecid

Lab Tests: Coombs' test, aspartate aminotransferase

Administrative Notes: Patients with kidney problems may require a reduction in dose

Dicumarol

Trade Name(s): Generic only

Chemically Related To: Warfarin

Pregnancy Category: X

Medical Category: Anticoagulant

Accepted Indications: Thrombosis, thromboembolism, pulmonary embolism

Mechanism of Action: Inhibits vitamin K-dependent precursors that prevent the formation of active coagulation factors

Absorption/Distribution: Slowly and incompletely absorbed from GI tract

Half life: 1–{endash}4 d dose dependent

PO: Onset of action, 1–{endash}5 d; duration of action, 2–{endash}10 d

Metabolism: Hepatic

Elimination: Renal

Research Notes: Patient compliance is essential to the safe use of this medication

Adult Dosage: Oral 25–{endash}200 mg/d as indicated by prothrombin-time measurement

Elderly Dosage: Decrease dosage

Child Dosage: Not established

Infant Dosage: Not established

Dosage Forms: Tablets: 25 mg and 50 mg

By System: Liver cells

Warnings: Carry identification indicating use of anticoagulant; elderly may require decreased dosage

Precautions: Have regular prothrombin time tests; keep a record of missed doses

Frequent Side Effects: Diarrhea, bloated stomach or gas

Occasional Side Effects: Leukopenia, nausea or vomiting, stomach cramps, loss of appetite, unusual hair loss

Rare Side Effects: Acute adrenal insufficiency, agranulocytosis, hepatotoxicity, renal damage

Contraindications: Active bleeding, cerebrovascular hemorrhage, hemophilia, severe hypertension, major surgery

Overdosage: Bleeding from gums during tooth brushing; unexplained bruising; unexplained bleeding episodes

Antidotal Therapy: May include administration of vitamin K PO or IV; transfusion of fresh frozen plasma or prothrombin complex

Disease States: Severe diabetes, GI ulceration, renal impairment, active tuberculosis, vitamin C or K deficiency

Nutrition: Avoid green, leafy vegetables

Other Drugs: Acetaminophen, anabolic steroids, aspirin, oral contraceptives, chloramphenicol, estrogens, methyldopa, quinidine, allopurinol, antibiotics, disulfiram, NSAIDs, metromidazole, rifampin

Administrative Notes: Seek professional advice before taking vitamin K containing vitamins or nutritional supplements because of alteration of anticoagulant effects

Dicyclomine Hydrochloride

Trade Name(s): Antispas, A-Spas, Bentyl, Di-Spaz, Dibent, Neoquess, Or-Tyl, Spasmoject

Chemically Related To: Antihistamines

Medical Category: Anticholinergic, antispasmodic

Accepted Indications: Irritable bowel syndrome

Unaccepted Indications: Peptic ulcer

Mechanism of Action: Affects smooth muscle in GI tract to reduce tone and motility

Half life: 1.8 h elimination (initial phase), 9–{endash}10 h (secondary phase)

PO: Absorbed from GI tract

Metabolism: Hepatic

Elimination: Renal, fecal

Adult Dosage: Capsules or tablets: 10–{endash}20 mg t.i.d. or q.i.d., up to 160 mg/d; syrup: 10-20 mg t.i.d. or q.i.d., up to 160 mg/d; injection: 20 mg every 4–{endash}6 h

Elderly Dosage: Same as adult dose

Child Dosage: Capsules or tablets, up to 6 y: not recommended; 6 y and over: 10 mg t.i.d. or q.i.d. Syrup: 10 mg t.i.d. or q.i.d. Injection: not established.

Infant Dosage: Capsules or tablets: not recommended; Syrup: up to 6 m: not recommended; 6 m–{endash}2 y: 5–{endash}10 mg t.i.d. or q.i.d. Injection: not established.

Dosage Forms: Capsules: 10 mg and 20 mg: syrup: 10 mg/5 mL; tablets: 20 mg; injection: 10 mg/mL

By System: GI tract

Precautions: Not recommended in infants under 3 m because respiratory symptoms, as well as seizures, syncope, asphyxia, pulse rate fluctuations, hypotonia, and coma, have been reported in some infants 3 m and under

Frequent Side Effects: Constipation; decreased sweating; dry mouth; redness or other signs of irritation at injection site

Occasional Side Effects: Decreased flow of breast milk; decreased salivary secretion; difficulty in accommodation of the eye; mydriatic effect

Rare Side Effects: Confusion, increased intraocular pressure; orthostatic hypotension; sensation of bloating; difficulty in urination; drowsiness; headache; lightheadedness; loss of memory; nausea; extreme tiredness; allergic reaction

Overdosage: Blurred vision; clumsiness; confusion; difficulty in breathing; dizziness; drowsiness; dry mouth, nose, or throat; tachycardia; fever; hallucinations; severe muscle weakness; seizures; slurred speech; extreme tiredness; extreme excitement, restlessness, or irritability; unusual warmth; dryness and flushing of skin

Disease States: Cardiac disease, brain damage in children, reflux esophagitis, Down syndrome, fever, GI tract obstructive disease, glaucoma, acute hemorrhage, hiatal hernia, intestinal atony, hepatic function impairment, hypertension, hyperthyroidism, myasthenia gravis, prostatic hypertrophy, urinary retention, uropathy, pyloric obstruction, tachycardia, ulcerative colitis, paralytic ileus, chronic lung disease, autonomic neuropathy, renal function impairment, spastic paralysis, toxemia of pregnancy, xerostomia

Other Drugs: Antacids, antidiarrheals, anticholinergics, carbonic anhydrase inhibitors, citrates, sodium bicarbonate, antimyasthenics, holoperidol, metoclopramide, opioid analgesics, cyclopropane, ketoconazole, potassium chloride

Lab Tests: Gastric acid secretion test

Didanosine

Trade Name(s): Videx

Pregnancy Category: B

Medical Category: Systemic antiviral

Accepted Indications: Advanced HIV, AIDS

Mechanism of Action: Inhibits HIV DNA polymerase

Half life: 1.5 h

PO: 0.5–{endash}1 h

Metabolism: Intracellular

Elimination: Renal

Adult Dosage: Oral solution and tablets: 125–{endash}200 mg b.i.d. Buffered oral suspension: not used by adults and adolescents.

Elderly Dosage: May require lower dose

Child Dosage: Buffered oral suspension and tablets: 25–{endash}125 mg b.i.d. or t.i.d. Oral solution: not prescribed for children.

Infant Dosage: Same as child dose

Dosage Forms: Oral solution: 100 mg, 167 mg, 250 mg, and 375 mg. Buffered oral suspension: 2000 mg/200 mL and 4000 mg/400 mL. Tablets: 25 mg, 50 mg, 100 mg, and 150 mg.

Warnings: Do not swallow tablets whole

Frequent Side Effects: Peripheral neuropathy, CNS toxicity, dry mouth, GI disturbances

Occasional Side Effects: Pancreatitis

Rare Side Effects: Anemia, leukopenia, seizures, cardiomyopathy, hepatitis, thrombocytopenia, hypersensitivity, retinal depigmentation

Contraindications: Alcoholism, pancreatitis

Disease States: Gout, renal impairment, liver impairment, hypertriglyceridemia, sodium-restriction conditions, peripheral neuropathy

Other Drugs: Lithium, alcohol, estrogens, ketoconazole, asparaginase, azathioprine, furosemide, methyldopa, sulindac, valproic acid, nitrofurantoin, pentamidine, sulfonamides, tetracycline, thiazide diuretics, fluoroquinolone antibiotics, itraconazole, dapsone, chloramphenicol, cisplatin, ethambutol, ethionamide, isoniazid, hydralazine, metronidazole, nitrous oxide, phenytoin, stavudine, zalcitabine

Lab Tests: Serum amylase, lipase, potassium

Dienestrol

Trade Name(s): Dv, Ortho Dienestrol

Chemically Related To: Diethylstilbestrol

Pregnancy Category: X

Medical Category: Estrogen (vaginal)

Accepted Indications: Atrophic vaginitis, vulvar squamous hyperplasia

Mechanism of Action: Reduces release of FSH and LH

Absorption/Distribution: Extensively absorbed (50%) into the systemic circulation; distributed to most tissues; high affinity for adipose tissue

Metabolism: Hepatic

Elimination: Renal

Research Notes: Estrogen therapy should be administered at lowest effective dose

Adult Dosage: Initial: intravaginal, 1 applicatorful once daily or b.i.d. for 1–{endash}2 w

Elderly Dosage: Same as adult dose

Dosage Forms: Cream, 0.01%

By System: Vaginal

Precautions: Use medication at bedtime to increase effectiveness; wear sanitary napkin to protect clothing

Frequent Side Effects: Breast pain or tenderness, enlargement of breasts, abdominal cramping, anorexia

Occasional Side Effects: Diarrhea, dizziness, headache, migraine headache

Rare Side Effects: Amenorrhea, breakthrough bleeding, breast tumors

Contraindications: Breast cancer, abnormal vaginal bleeding

Disease States: Endometriosis, gallbladder disease, hepatic dysfunction, thrombophlebitis, uterine fibroids

Other Drugs: Adrenocorticoids, bromocriptine, cyclosporine, tamoxifen, hepatotoxic medication

Lab Tests: Fasting blood glucose, glucose tolerance, thyroid function, calcium, prolactin, prothrombin, renin substrate, antithrombin III

Diethylpropion Hydrochloride

Trade Name(s): M-Orexic, Tenuate, Tepanil

Chemically Related To: Amphetamines

Scheduled Class: IV

Abuse Potential: Minor

Pregnancy Category: B

Medical Category: Appetite suppressant

Accepted Indications: Exogenous obesity, infantile autism

Mechanism of Action: Releases norepinephrine from nerve terminals in the brain

Half life: 4–{endash}6 h

Metabolism: Hepatic

Elimination: Renal

Research Notes: Duration of action 4 h

Adult Dosage: 25 mg t.i.d., 1 h before meals

Elderly Dosage: No information available

Child Dosage: Up to 12 y: not recommended

Infant Dosage: Not recommended

Dosage Forms: Tablets: 25 mg; extended-release tablets: 75 mg

By System: CNS

Warnings: May cause dizziness; elderly may require decreased dose

Precautions: Caution if surgery required

Frequent Side Effects: Elevated blood pressure, CNS stimulation

Occasional Side Effects: Blood dyscrasias, mental depression, pulmonary hypertension

Rare Side Effects: Blurred vision, constipation, nausea/vomiting

Contraindications: Agitated states, alcoholism, arteriosclerosis, drug abuse, glaucoma, hyperthyroidism

Overdosage: Stomach cramps, arrhythmias, confusion, diarrhea, fever, hallucinations, nausea/vomiting, tremor

Antidotal Therapy: No specific antidote; supportive measures including emesis/gastric lavage, barbiturates, IV fluids, IV phentolamine

Disease States: Cardiovascular disease, diabetes mellitus, epilepsy, psychosis

Other Drugs: Alcohol, hydrocarbon anesthetics, insulin, antihypertensives, CNS-stimulating hormones, MAO inhibitors, phenothiazines

Administrative Notes: If tolerance develops, medication should be discontinued

Diethylstilbestrol

Trade Name(s): Generic only

Chemically Related To: Ethinyl estradiol

Pregnancy Category: X; daughters of women who took diethylstilbestrol during pregnancy have developed cancer of the vagina in later life

Medical Category: Estrogen, antineoplastic, antiosteoporotic

Accepted Indications: Estrogen deficiency, atrophic vaginitis, ovarian failure, breast cancer, prostatic cancer

Unaccepted Indications: Postpartum breast engorgement, postcoital contraception

Mechanism of Action: Estrogen replacement and reduces the release of FSH and LH

Metabolism: Hepatic

Elimination: Renal

Research Notes: Also known as DES; may predispose patient to gingival bleeding

Adult Dosage: 1–{endash}15 mg/d

Dosage Forms: Enteric-coated tablets: 1 mg and 5 mg

By System: Endocrine system

Warnings: If pregnancy is suspected, stop medication immediately

Precautions: Possibility of dental problems, bleeding gums

Frequent Side Effects: Breast pain or tenderness, peripheral edema, anorexia, abdominal cramping, nausea

Occasional Side Effects: Diarrhea, dizziness, headache, migraine headaches, menstrual alteration

Rare Side Effects: Amenorrhea, gallbladder obstruction, hepatitis, breast tumors, thrombophlebitis

Contraindications: Breast cancer, abnormal vaginal bleeding

Disease States: Endometriosis, gallbladder disease, jaundice, thrombophlebitis, uterine fibroids

Other Drugs: Adrenocorticoids, bromocriptine, corticotropin, cyclosporine, hepatotoxic medications, tamoxifen

Lab Tests: Fasting blood glucose; glucose tolerance; calcium; coagulation factors VII, VIII, IX, and X; glucose

Administrative Notes: The use of large doses of estrogens in males to treat breast and prostate cancer has been associated with an increased risk of myocardial infarction, pulmonary embolism, and thrombophlebitis

Difenoxin Hydrochloride

Trade Name(s): Not available as a single agent

Chemically Related To: Diphenoxylate

Scheduled Class: IV

Abuse Potential: Minor

Pregnancy Category: C

Medical Category: Antidiarrheal

Accepted Indications: Diarrhea

Mechanism of Action: Reduces intestinal motility

Half life: 4.5 hours

PO: 40–{endash}60 min

Metabolism: Hepatic

Elimination: Renal/fecal

By System: GI tract

Diflorasone Diacetate

Trade Name(s): Florone, Maxiflor, Psorcon

Pregnancy Category: C

Medical Category: Topical corticosteroid, topical steroidal anti-inflammatory

Accepted Indications: Skin disorders

Unaccepted Indications: Acne, rosacea

Metabolism: Skin, hepatic

Adult Dosage: Topical, to the skin once daily–{endash}q.i.d.

Elderly Dosage: Lower dose may be required

Child Dosage: Topical, to the skin, once daily

Dosage Forms: Cream: 0.05%. Ointment: 0.05%.

Occasional Side Effects: Folliculitis, numbness in fingers, skin atrophy, contact dermatitis, furunculosis, purpura, secondary skin infection

Rare Side Effects: Cushing's syndrome, gastric ulcer, hirsutism, acneiform eruptions, cataracts, glaucoma, perioral dermatitis, ecchymosis, edema, hypertension, hypopigmentation, skin maceration, loss of scalp hair

Contraindications: Infection at site, skin atrophy, herpes simplex

Disease States: Cataracts, diabetes, glaucoma, tuberculosis

Lab Tests: ACTH, hypothalamic-pituitary-adrenal axis

Diflunisal

Trade Name(s): Dolobid

Chemically Related To: Aspirin

Pregnancy Category: C

Medical Category: Antirheumatic, analgesic, vascular headache suppressant, antigout agent

Accepted Indications: Rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, pain, vascular headache, gouty arthritis

Mechanism of Action: Inhibits formation of precursors of prostaglandins

Absorption/Distribution: Rapid and complete absorption

Half life: 1.2–{endash}2 h (elimination)

PO: 2–{endash}3 h

Metabolism: Hepatic

Elimination: Renal, biliary

Research Notes: Onset of action, 1 h; duration of action, 8–{endash}12 h

Adult Dosage: 250 mg–{endash}500 mg b.i.d.

Elderly Dosage: Lower dose may be required

Child Dosage: Safety and efficacy not established

Infant Dosage: Safety and efficacy not established

Dosage Forms: Tablets: 250 mg and 500 mg

By System: CNS and peripheral pain receptors

Warnings: Enhances GI ulceration and bleeding; avoid alcohol

Frequent Side Effects: Rash, headache, stomach cramps, diarrhea, heartburn, nausea

Occasional Side Effects: Tinnitus; dizziness; drowsiness; insomnia; extreme tiredness; gas; constipation; vomiting; dry mouth

Rare Side Effects: Gastritis, cystitis, agranulocytosis, thrombocytopenia, hepatitis, muscle cramps or pain, blurred vision, fluid retention, shortness of breath, chest pain, confusion, hallucinations, disorientation, mental depression, peripheral neuropathy, syncope, dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, GI bleeding, GI perforation, GI ulceration, dysuria, cloudy urine, hemolytic anemia, anaphylaxis, angioedema, hypersensitivity, stomatitis, interstitial nephritis, nephrotic syndrome, renal impairment, increased sweating, pounding heartbeat, vertigo, nervousness, photosensitivity, decreased appetite, Reye's syndrome in children

Contraindications: Symptoms of nasal polyps associated with bronchospasm or angioedema induced by aspirin or other NSAIDs

Antidotal Therapy: May include support of vital functions and treatment of symptoms

Disease States: Anemia, hypertension, sepsis, hemophilia, hepatic and/or renal impairment, stomatitis, systemic lupus erythematosus, GI inflammatory disease

Other Drugs: Acetaminophen, potassium supplements, antacids, anticoagulants, antidiabetic agents, antihypertensives, colchicine, gold compounds, heparin, thrombolytic agents, indomethacin, aspirin, cefamandole, cefoperazone, cefotetan, plicamycin, valproic acid, cyclosporine

Lab Tests: BUN, liver function tests, ophthalmologic examinations, upper GI diagnostic tests, hematologic determinations, hematocrit

Digitoxin

Trade Name(s): Crystodigin

Chemically Related To: Digitalis

Pregnancy Category: C

Medical Category: Antiarrhythmic, cardiotonic

Accepted Indications: Cardiac arrhythmias, CHF, cardiogenic shock

Unaccepted Indications: Obesity

Mechanism of Action: Positive inotropic action, decreased conduction rate

Absorption/Distribution: Almost completely absorbed

Half life: 120–{endash}216 h

PO: 8–{endash}14 h

Metabolism: Hepatic

Elimination: Renal

Research Notes: Onset of action, 1–{endash}4 h; duration of action, 14 h

Adult Dosage: Digitalization: up to 1.6 mg over 1–{endash}2 d. Maintenance dose: 50–{endash}300 m{mu}g/d

Elderly Dosage: Lower doses required

Child Dosage: Other digitalis glycosides should be considered

Infant Dosage: Premature and immature infants especially sensitive

Dosage Forms: Tablets: 100 m{mu}g and 200 m{mu}g

By System: Cardiovascular

Warnings: Keep out of reach of children; do not take other medicines without advice from physician

Precautions: Carry medical identification card; caution if medical or dental surgery or emergency treatment is required

Frequent Side Effects: Headache, nausea

Occasional Side Effects: Loss of appetite, nausea/vomiting, diarrhea, electrolyte imbalance, blurred vision, drowsiness, mental depression, headache, fainting, arrhythmia

Rare Side Effects: Rash

Contraindications: Ventricular fibrillation

Antidotal Therapy: May include sodium bicarbonate; protection of patient's airway; activated charcoal. Correct arrhythmias, correct hypokalemia, consider digoxin immune Fab for serious overdose

Disease States: Hyperkalemia, myocardial infarction, hypokalemia, premature ventricular contractions, ventricular tachycardia, atrioventricular block

Other Drugs: Diuretics, adrenocorticoids, carbonic anhydrase inhibitors, sympathomimetics, calcium channel blockers, potassium salts, quinidine, spironolactone, verapamil, quinidine

Lab Tests: EKG

Administrative Notes: Store in sealed container; dosage calculations should be based on lean body weight because drug is not taken up by adipose tissue; monitor patient

Digoxin

Trade Name(s): Lanoxicaps, Lanoxin

Chemically Related To: Digitoxin

Pregnancy Category: C

Medical Category: Antiarrhythmic, cardiotonic

Accepted Indications: Arrhythmias, CHF, cardiogenic shock

Unaccepted Indications: Obesity

Mechanism of Action: Increases intracellular myocardial Ca2+{plus}, decreases the conduction rate, and increases the effective refractory period of the AV node, resulting in increased contractile force and slower rate

Absorption/Distribution: Bioavailability is 60–{endash}80% (tablets), 70–{endash}85% (oral elixir or IM injection), 90–{endash}100% (capsules)

Half life: IV 36–{endash}48 hours; oral 4–{endash}6 days

PO: 2–{endash}6 hours

IV: 5–{endash}30 minutes

Metabolism: Minimal hepatic

Elimination: Renal

Research Notes: In some patients, digoxin is converted to inactive products by colonic bacteria in the gut. Onset of action is 5–{endash}30 min after IV, 30 min–{endash}2 h after oral administration

Adult Dosage: Digitalization 50–{endash}350 m{mu}g/d in divided doses for 2 d; maintenance 50–{endash}350 m{mu}g/d

Elderly Dosage: May require decreased doses to avoid toxicity; loss of appetite is a risk

Child Dosage: Digitalizing dose: 2–{endash}5 years: oral, 25–{endash}35 m{mu}g/kg/d; 5–{endash}10 years: oral, 15–{endash}30 m{mu}g/kg/d; 10 years and over: oral 8–{endash}12 m{mu}g/kg/d. Maintenance dose: up to 10 years: oral, 25–{endash}35% of the digitalizing dose divided and administered in 2 or 3 equal doses/d; 10 years and over: oral, 25–{endash}35% of the digitalizing dose administered once a day

Infant Dosage: Digitalizing dose: premature neonates: oral, 15–{endash}25 m{mu}g/kg/d; full-term neonates: oral, 20–{endash}30 m{mu}g/kg/d; 1 month–{endash}2 years: oral 30–{endash}50 m{mu}g/kg/d. Maintenance dose: premature neonates: oral, 20–{endash}30% of the total digitalizing dose, divided and administered in 2 or 3 equal doses/d; full-term neonates, infants: oral, 25–{endash}35% of the digitalizing dose divided and administered in 2 or 3 equal doses/d

Dosage Forms: Capsules: 50 m{mu}g, 100 m{mu}g, and 200 m{mu}g; elixir: 50 m{mu}g/mL; tablets: 125 m{mu}g, 250 m{mu}g, and 500 m{mu}g; injection: 100 m{mu}g/mL and 250 m{mu}g/mL

By System: Cardiovascular

Precautions: Carry medical identification card; caution if medical or dental surgery or emergency treatment is required

Frequent Side Effects: Dizziness, nausea, and vomiting; arrhythmia

Occasional Side Effects: Halo vision

Rare Side Effects: Gynecomastia

Contraindications: Ventricular fibrillation

Overdosage: Nausea and vomiting, lower stomach pain, diarrhea, electrolyte imbalance, bradycardia or arrhythmia, visual disturbances such as halo vision

Antidotal Therapy: May include activated charcoal, potassium salts; lidocaine or similar drug to correct arrhythmias; digoxin Immune Fab for serious overdose

Disease States: AV block, hepatic function impairment, myocardial infarction, severe pulmonary disease, ventricular tachycardia

Other Drugs: Beta-adrenergic blocking agents or other antiarrhythmics may cause additive bradycardia. Half-life is increased with spironolactone. Antacids, kaolin-pectin, cholestyramine, or colestipol may decrease absorption. Therapeutic effects may be decreased by thyroid hormones. Potassium-depleting diuretics, antacids, sympathomimetics, calcium channel blockers, captopril, heparin, erythromycin, potassium salts, thyroid hormones, propafenone, quinidine

Lab Tests: EKG

Dihydroergotamine Mesylate

Trade Name(s): D.H.E. 45

Chemically Related To: Ergotamine

Pregnancy Category: Use not recommended

Medical Category: Vascular headache suppressant

Accepted Indications: Vascular headache, cluster headache, thrombosis, prophylaxis adjunct, hypotension

Unaccepted Indications: Migraine, long-term therapy

Mechanism of Action: Causes constriction of arteries and veins, depresses vasomotor centers

Absorption/Distribution: Rapid

Half life: Distribution 1–{endash}4 min (IV), 1 h (SQ); elimination half-life 18–{endash}32 h

IM: 15 min–{endash}2 h

IV: 15 min–{endash}2 h

Metabolism: Hepatic

Elimination: Hepatic, biliary

Research Notes: IM onset of action, 15–{endash}30 min; IV onset of action, 5 min; IV and SQ duration of action, 8 h

Adult Dosage: Acute migraine or cluster headache, IM: 1 mg at start of attack, may repeat in 1 h, maximal dose of 3 mg; IV: 0.5 mg at start of attack, may repeat in 1 h, maximal dose of 2 mg, 6 mg/w maximum. Chronic intractable headache, IV: 0.5 mg administered over 1 min, 3–{endash}5 min after IV administration of an antiemetic, up to 1 mg may be given for subsequent doses if needed, regimen may be repeated q8h

Elderly Dosage: Caution recommended

Child Dosage: 6 y and over: IM, 0.5 mg at start of attack, may be repeated in 1 h; IV, 0.25 mg at start of attack, may be repeated in 1 h. Under 6 y: not recommended

Infant Dosage: Not recommended

Dosage Forms: Injection: 1 mg/mL

By System: Vascular

Frequent Side Effects: Edema, CNS effects, dry mouth, diarrhea, nausea, vomiting, peripheral vascular effects

Occasional Side Effects: Angina; tachycardia or bradycardia; hypertension or hypotension; rapid, weak pulse; ischemia; ocular vasospasm

Overdosage: CNS toxicity, vomiting, diarrhea, respiratory depression, stomach pain or bloating

Antidotal Therapy: May include discontinuation, benzodiazepines, volume expanders

Disease States: Coronary artery disease, angina, hypertension, sepsis, trauma, angioplasty, vascular surgery, hepatic function impairment, pruritus, renal function impairment

Other Drugs: Macrolides, vasoconstrictors, ergot alkaloids, nitroglycerin, beta blockers

Dihydrotachysterol

Trade Name(s): DHT, DHT Intensol, Hytakerol

Chemically Related To: Vitamin D

Pregnancy Category: C

Medical Category: Antihypocalcemic, antihypoparathyroid

Accepted Indications: Hypocalcemia, hypophosphatemia, osteodystrophy, rickets

Unaccepted Indications: Psoriasis

Mechanism of Action: Increases serum calcium; mobilizes calcium from bones

Absorption/Distribution: Readily absorbed from small intestine

Metabolism: Hepatic

Elimination: Biliary/renal

Research Notes: Dihydrotachysterol is stored mainly in the liver and other fat depots

Adult Dosage: All forms: 200 m{mu}g–{endash}2.5 mg/d

Child Dosage: All forms: 500 m{mu}g–{endash}5 mg/d

Infant Dosage: Some infants may be sensitive even to small doses

Dosage Forms: Capsules: 125 m{mu}g; oral solution: 200 m{mu}g/ml; tablets: 125 m{mu}g, 200 m{mu}g, and 400 m{mu}g

Contraindications: Hypercalcemia, hypervitaminosis D, renal osteodystrophy with hyperphosphatemia

Overdosage: Dry mouth, headache, cardiac arrhythmia, metallic taste, nausea or vomiting

Antidotal Therapy: May include small doses of potassium for cardiac arrhythmias

Disease States: Arteriosclerosis, cardiac and renal impairment, hyperphosphatemia, sarcoidosis

Other Drugs: Aluminum–{endash}containing antacids; anticonvulsants; barbiturates; diuretics; corticosteroids; digitalis glycosides

Lab Tests: Serum cholesterol, calcium, magnesium, alkaline phosphatase

Administrative Notes: The effectiveness of megadoses for treatment of various medical conditions is unproven, and their use should be discouraged

Diltiazem Hydrochloride

Trade Name(s): Cardizem

Chemically Related To: Benzothiazepines

Scheduled Class: N/A

Pregnancy Category: C

Medical Category: Antihypertensive, antianginal agent, antiarrhythmic

Accepted Indications: Hypertension, angina pectoris, supraventricular tachycardia

Mechanism of Action: Relaxes blood vessels, which decreases tone; slows heart rate; decreases contractile force as a result of less Ca2+{plus} activity inside cell

Absorption/Distribution: Well absorbed; undergoes first-pass effect

Half life: Early phase, 20–{endash}30 min; terminal phase, 3.5 h

Peak activity: 2–{endash}3 h

PO: 2–{endash}3 h

IV: Immediate

Metabolism: Hepatic

Elimination: Biliary and renal

Adult Dosage: Tablets and capsules, 120–{endash}360 mg/d, injection 250 m{mu}g/kg, followed by 350 m{mu}g/kg 15 min after initial dose if necessary

Elderly Dosage: May require decreased dose

Child Dosage: Not established

Infant Dosage: Not established

Dosage Forms: Tablets: 30 mg, 60 mg, 80 mg, and 120 mg; extended-release capsules: 60 mg, 90 mg, 120 mg, 180 mg, 240 mg, and 300 mg; injection: 5 mg/mL

By System: Vasodilator, cardiac depressant

Precautions: Caution in patients with impaired hepatic or renal function and patients with arrhythmias

Frequent Side Effects: Constipation, dizziness, flushing, headache, nausea and vomiting

Occasional Side Effects: Dyspnea; bradycardia; swelling of ankles, feet, etc.

Rare Side Effects: Tender or swollen gums, fainting, chest pain, swollen joints

Contraindications: Sick sinus syndrome

Overdosage: Hypotension, bradycardia

Antidotal Therapy: May include supportive measures

Disease States: Renal or hepatic disease, heart or vessel disorder

Other Drugs: Carbamazepine, cyclosporine, quinidine, digitalis

Lab Tests: SGOT/SGPT

Dimenhydrinate

Trade Name(s): Calm X, Dimetabs, Dinate, Dramamine, Dramanate, Dramoject, Dymenate, Hydrate, Marmine, Triptone, Vertab

Chemically Related To: Ethanolamine

Pregnancy Category: B

Medical Category: Antihistaminic, antiemetic, antivertigo, sedative-hypnotic

Accepted Indications: Rhinitis, pruritus, urticaria, vertigo, conjunctivitis, angioedema, dermatographism, sneezing, rhinorrhea, anaphylactic reactions, motion sickness

Mechanism of Action: Competes for H1 receptors, diminishes vestibular stimulation

Absorption/Distribution: Well absorbed after oral administration

Metabolism: Hepatic, renal

Elimination: Renal

Adult Dosage: PO: 50–{endash}100 mg q4h, up to 400 mg daily; injection: 50 mg q4h

Elderly Dosage: May require lower dose

Child Dosage: PO: 5 mg/kg in 4 divided doses, up to 300 mg/d; injection: 1.25 mg/kg q.i.d., up to 300 mg/d

Infant Dosage: Same as child dose

Dosage Forms: Capsules: 50 mg; elixir: 12.5 mg/5mL; tablets: 50 mg; syrup: 12.5 mg/4 mL and 15.62 mg/mL; chewable tablets: 50 mg; injection: 50 mg/mL

Frequent Side Effects: Drowsiness, thickening of mucus

Occasional Side Effects: Arrhythmias, blood dyscrasis, blurred vision, confusion, painful urination, dry mouth, tachycardia, increased sweating, loss of appetite, paradoxical reaction, photosensitivity, tinnitus, rash, GI upset

Contraindications: Urinary retention, glaucoma

Overdosage: Anticholingeric effects, cardiac arrhythmias, CNS depression, CNS stimulation, hypotension

Antidotal Therapy: May include emesis, gastric lavage, saline cathartics, vasopressors

Disease States: Bladder neck obstruction, prostatic hypertrophy

Other Drugs: Alcohol, CNS depressants, anticholinergics, MAO inhibitors, ototoxic medications

Lab Tests: Amylase, prolactin

Dimercaprol

Trade Name(s): BAL in oil

Pregnancy Category: C

Medical Category: Chelating agent

Accepted Indications: Arsenic toxicity, gold toxicity, mercury toxicity, lead toxicity (treatment adjunct)

Unaccepted Indications: Iron, cadmium, selenium, silver, or uranium poisoning, methylmercury intoxication, arsine gas poisoning

Mechanism of Action: Chelates metal and prevents or reverses its toxic effects

Absorption/Distribution: Distribution to all tissues

Elimination: Renal, biliary

Research Notes: Onset of action 30 min, duration of action 4 h

Adult Dosage: 3 mg/kg q4h for 2 d, 4 times on day 3, then b.i.d. for 10 d

Child Dosage: IM: 75 mg/m>sup>2 q4h for 5 d

Dosage Forms: Injection: 100 mg/mL

Frequent Side Effects: Tachycardia, fever, increased blood pressure, burning feeling, conjunctivitis, nausea, vomiting, runny nose, sweating, watery eyes and mouth, unpleasant breath odor

Occasional Side Effects: Injection abscesses, abdominal pain, tremors

Contraindications: Arsine gas poisoning, organic mercury poisoning, iron, cadmium, silver, selenium, or uranium poisoning

Overdosage: Convulsions, severe vomiting, severe drowsiness

Disease States: Hypertension, hepatic function impairment, renal function impairment, renal insufficiency

Other Drugs: Iron salts

Lab Tests: BUN, fluid balance

Dinoprostone

Trade Name(s): Prepidil, Prostin E2

Pregnancy Category: C

Medical Category: Prostaglandin, abortifacient, oxytocic, antihemorrhagic

Accepted Indications: Elective abortion, cervical ripening, postpartum hemorrhage, labor inducement, incomplete abortion, hydatidiform mole

Mechanism of Action: Stimulates myometrial contraction

Half life: Less than 1 min (elimination)

Peak activity: Mean abortion time 12–{endash}24 h

Metabolism: Local tissues, maternal lungs, kidney, spleen

Elimination: Renal

Adult Dosage: Intravaginal, 20 mg repeated q3–{endash}5h; maximum cumulative dose of 240 mg

Dosage Forms: Vaginal suppositories: 20 mg

Frequent Side Effects: Nausea, vomiting, abdominal cramps, diarrhea, fever

Occasional Side Effects: Chills, headache, anaphylaxis, peripheral vasoconstriction, bradycardia, bronchoconstriction, uterine pain, tachycardia, uterine hypertonus, substernal pressure

Rare Side Effects: Flushing, vulvar edema, ileus

Contraindications: Asthma, fetal malpresentation, active cardiac disease

Disease States: Pelvic inflammatory disease, anemia, hypertension, glaucoma, hepatic disease, renal disease, pulmonary disease

Other Drugs: Oxytocin

Lab Tests: Blood pressure

Diphenhydramine Hydrochloride

Trade Name(s): Banophen, Benadryl, Genahist, Nordryl

Chemically Related To: Ethanolamines

Pregnancy Category: B

Medical Category: Antihistaminic (H1-receptor), antidyskinetic, antiemetic, antitussive, antivertigo, sedative-hypnotic

Accepted Indications: Rhinitis, conjunctivitis, pruritus, urticaria, angioedema, anaphylactic reactions, anxiety, extrapyramidal reactions, cough, vertigo, insomnia,

Mechanism of Action: Competes with histamine for receptor site (H1)

Absorption/Distribution: Well absorbed

Half life: 1–{endash}4 h

PO: 1–{endash}4 h

Metabolism: Hepatic, renal

Elimination: Renal

Research Notes: Duration of action 6–{endash}8 h

Adult Dosage: 25–{endash}50 mg every 4–{endash}6 h up to 300 mg/d

Elderly Dosage: Half the adult dosage

Child Dosage: Up to 6 y: 6.25–{endash}12.5 mg every 4–{endash}6 h; 6–{endash}12 y: 12.5–{endash}25 mg every 4–{endash}6 h not to exceed 100 mg

Infant Dosage: Not recommended in newborn or premature infants

Dosage Forms: Capsules: 25 mg and 50 mg; elixir: 12.5 mg/5 mL; syrup 12.5 mg/5 mL; tablets: 25 mg and 50 mg; injection: 10 mg/mL and 50 mg/mL

By System: Systemic

Warnings: May cause drowsiness; avoid alcohol

Precautions: Use sugarless gum or candy for dry mouth

Frequent Side Effects: Drowsiness, thick mucus

Occasional Side Effects: Blood dyscrasias, cardiac arrhythmias

Rare Side Effects: Blurred vision, confusion, dry mouth, loss of appetite, tinnitus, excitement

Contraindications: Liver problems

Overdosage: Anticholinergic effects, cardiac arrhythmias, CNS depression/stimulation, hypotension

Antidotal Therapy: No specific antidote; may include emesis/gastric lavage, saline cathartics, vasopressors, oxygen, IV fluids

Disease States: Glaucoma, bladder neck obstruction, urinary retention, prostatic hypertrophy

Other Drugs: CNS depressants, anticholinergics, erythromycin, MAO inhibitors, ototoxic medications, ketoconazole

Lab Tests: Skin tests with allergen extracts

Administrative Notes: Protect elixir and injection solution from light

Diphenidol Hydrochloride

Trade Name(s): Vontrol

Chemically Related To: Indolamines

Pregnancy Category: Safety not established

Medical Category: Antiemetic, antivertigo

Accepted Indications: Vertigo, nausea and vomiting associated with disease states

Unaccepted Indications: Treatment of ventricular tachyarrhythmias, nausea and vomiting associated with pregnancy

Mechanism of Action: Diminishes vestibular stimulation and depresses labyrinthine function

Absorption/Distribution: Well absorbed

Half life: 4 h

PO: 1.5–{endash}3 h

Elimination: Renal

Research Notes: Has little sedative, tranquilizing, or antihistaminic action; a weak peripheral anticholinergic effect

Adult Dosage: 100–{endash}300 mg/d in 4–{endash}6 divided doses

Child Dosage: Up to 22.8 kg: not recommended; 22.8–{endash}45.6 kg: 25 mg every 4 h; 22.8 kg and over: 5.5 mg/kg/d

Infant Dosage: Not recommended

Dosage Forms: Tablets: 25 mg

By System: CNS subcortical nuclei

Warnings: May cause drowsiness; avoid CNS depressants

Precautions: Because of its potential to cause hallucinations, disorientation, and confusion, use should be limited

Frequent Side Effects: Drowsiness

Occasional Side Effects: Blurred vision, dizziness, dry mouth, headache, nervousness, restlessness

Rare Side Effects: Confusion, hallucinations, weakness

Contraindications: Anuria

Overdosage: Drowsiness, shortness of breath, extreme tiredness or weakness

Antidotal Therapy: May include supportive measures

Disease States: GI tract obstructive disease, glaucoma, hypotension, renal impairment

Other Drugs: Anticholinergics, apomorphine, CNS depressants

Diphenoxylate Hydrochloride

Trade Name(s): Not available as a single agent

Chemically Related To: Opioids

Scheduled Class: V

Abuse Potential: Low

Pregnancy Category: C

Medical Category: Antidiarrheal

Accepted Indications: Diarrhea management adjunct

Unaccepted Indications: Diarrhea caused by poisoning until poison eliminated

Mechanism of Action: Slows movement of the intestine

Absorption/Distribution: Well absorbed from GI tract

Half life: 2.5 h, 12–{endash}14 elimination

Metabolism: Hepatic, into difenoxin active metabolite

Elimination: Fecal/renal

By System: GI

Warnings: May cause drowsiness or dizziness; avoid alcohol

Antidotal Therapy: May include emesis/gastric lavage, respiratory support, naloxone

Disease States: Liver problems, drug abuse or dependency, gallbladder disease, hypothyroidism

Other Drugs: MAO inhibitors, barbiturates, tranquilizers, alcohol, naltrexone, opioid analgesics

Diphenoxylate/Atropine

Trade Name(s): Lomotil

Chemically Related To: Meperidine

Scheduled Class: V

Abuse Potential: Low

Pregnancy Category: C

Medical Category: Antidiarrheal

Dipyridamole

Trade Name(s): Dipridacot, Persantine

Chemically Related To: Pyrimidines

Pregnancy Category: B

Medical Category: Platelet aggregation inhibitor, antithrombotic adjunct, diagnostic aid adjunct, myocardial reinfarction, prophylatic adjunct

Accepted Indications: Platelet aggregation prophylaxis, myocardial perfusion imaging adjunct

Unaccepted Indications: Chronic angina pectoris long term treatment

Mechanism of Action: Inhibits platelet adhesion, relaxes coronary vessels

Absorption/Distribution: Low and variable; high protein binding

Half life: 10–{endash}15 h elimination

PO: 1–{endash}3 h

IV: 2 min after 4-min infusion

Metabolism: Hepatic

Elimination: Biliary

Adult Dosage: 75–{endash}100 mg q.i.d.

Elderly Dosage: Same as adult dosage

Dosage Forms: Tablets: 25 mg, 50 mg and 75 mg; injection: 5 mg/mL

By System: Hematopoietic, coronary vasculature

Warnings: May increase bleeding

Precautions: May cause hypotension

Frequent Side Effects: Angina, dizziness

Occasional Side Effects: Flushing, weakness, hypertension, tachycardia, allergic reaction, dyspnea, GI upset, diarrhea, nausea, hypertension, hypotension

Rare Side Effects: Bronchospasm, migraine

Overdosage: Hypotension

Antidotal Therapy: May include 50–{endash}250 mg aminophylline IV

Disease States: Angina, hypotension

Nutrition: May be taken with meals, which will slow absorption

Other Drugs: Streptokinase, urokinase, anticoagulants, NSAIDs, platelet aggregation inhibitors, valproic acid, adenosine, xanthines

Disopyramide Phosphate

Trade Name(s): Norpace, Rythmodan

Chemically Related To: Anticholinergics

Pregnancy Category: C

Medical Category: Antiarrhythmic

Accepted Indications: Ventricular arrhythmia, supraventricular tachycardia

Mechanism of Action: Stabilizes membrane of heart; prolongs action of potential

Absorption/Distribution: Rapid, complete absorption; moderate protein binding

Half life: 7 h

PO: 0.5–{endash}3 h

Metabolism: Hepatic

Elimination: Renal/biliary

Research Notes: Duration of action: 1.5–{endash}8.5 h

Adult Dosage: Maintenance: 150 mg q.i.d. up to 800 mg/d

Child Dosage: 1–{endash}4 y: 10–{endash}20 mg/kg/d; 4–{endash}12 y: 10–{endash}15 mg/kg/d; 12–{endash}18 y: 6–{endash}15 mg/kg/d

Infant Dosage: Up to 1 y: 10–{endash}30 mg/kg/d

Dosage Forms: Capsules: 100 mg and 150 mg; extended-release capsules: 100 mg, 150 mg, and 250 mg

By System: Cardiovascular

Warnings: May cause blurred vision; avoid alcohol; elderly patients and patients with impaired renal function may require decreased dosage

Precautions: Children should be hospitalized during early part of therapy

Frequent Side Effects: Anticholinergic effects

Occasional Side Effects: Chest pain, confusion, CHF, fluid retention, sensation of bloating, loss of appetite

Rare Side Effects: Agranulocytosis, headache, hunger, tachycardia, tiredness

Contraindications: AV block, cardiogenic shock

Overdosage: Apnea, loss of consciousness, cardiac arrhythmias, respiratory distress

Antidotal Therapy: No specific antidote; may include EKG monitoring, mechanical respirator, cardiac glycosides

Disease States: Bladder neck obstruction, CHF, diabetes mellitus, myasthenia gravis, liver and kidney problems, glaucoma

Other Drugs: Antiarrhythmics, anticoagulants, insulin, hepatic enzyme inducers, pimozide

Lab Tests: Blood glucose concentrations, EKG changes

Disulfiram

Trade Name(s): Antabuse

Chemically Related To: Sulfonamides

Pregnancy Category: Adequate studies in humans have not been done

Medical Category: Antialcoholism agent

Accepted Indications: Treatment of alcoholism

Mechanism of Action: Irreversible inhibition of enzyme aldehyde dehydrogenase, which increases concentration of acetaldehyde in blood, causing severe nausea

Absorption/Distribution: Absorption is slow

Half life: 8 h

PO: 60 min

Metabolism: Hepatic

Elimination: Renal

Research Notes: Disulfiram-alcohol reactions may occur up to 14 d after last dose of disulfiram

Adult Dosage: Initial: Up to 500 mg/d; maintenance: 125–{endash}500 mg (average 250 g) once daily

Elderly Dosage: May be more sensitive to effects of adult doses; hypotension possible; overdose may be fatal

Child Dosage: Safety and efficacy not established

Infant Dosage: Safety and efficacy not established

Dosage Forms: Tablets: 250 mg and 500 mg

By System: Hepatic enzymes

Warnings: Do not take this medication if blood alcohol level is not zero

Precautions: Check all liquid medications for presence of alcohol; patient should carry medical identification card during therapy

Frequent Side Effects: Drowsiness

Occasional Side Effects: Neurotoxicity, psychotic reaction, optic neuritis, numbness or tingling sensation in hands or feet

Rare Side Effects: Mental changes, hepatitis, headache, impotence, rash, extreme tiredness

Overdosage: Disulfiram-alcohol reaction: blurred vision, chest pain, confusion, dizziness or faintness, tachycardia, flushing, increased sweating, nausea and vomiting, throbbing headache, dyspnea, weakness

Antidotal Therapy: May include supportive measures

Disease States: Allergic eczematous contact dermatitis, cardiovascular disorders, depression, diabetes mellitus, epilepsy, hypothyroidism, psychosis, pulmonary insufficiency, hepatic and renal function impairment

Other Drugs: Alcohol, anticoagulants, anticonvulsants, tricyclic antidepressants

Lab Tests: Cholesterol concentrations

Administrative Notes: The patient should be made fully aware of the nature of this medicine and the disulfiram-alcohol reaction

Divalproex Sodium

Trade Name(s): Depakote

Chemically Related To: Valproic acid

Pregnancy Category: D

Medical Category: Anticonvulsant

Accepted Indications: Epilepsy, bipolar disorders

Mechanism of Action: Increases levels of inhibitory GABA

Absorption/Distribution: Enteric coating on tablet delays absorption by 1–{endash}4 h

Half life: 6–{endash}16 h

PO: 3–{endash}4 h

Metabolism: Hepatic

Elimination: Renal, fecal, respiratory

Adult Dosage: Delayed-release capsules: initally, 5–{endash}30 mg/kg/d, dosage increased at 1-w intervals up to 60 mg/kg/d

Elderly Dosage: Increased concentrations and lowered clearance

Child Dosage: 1–{endash}12 y: 15–{endash}100 mg/kg/d, dosage increased at 1-w intervals

Infant Dosage: 10–{endash}15 mg/kg/d

Dosage Forms: Capsules: the equivalent of valproic acid 125 mg; delayed-release tablets: the equivalent of valproic acid 125 mg, 250 mg, and 500 mg

By System: CNS

Warnings: May cause drowsiness; avoid alcohol

Precautions: Caution if surgery required

Frequent Side Effects: Stomach cramps, diarrhea, anorexia, hair loss, indigestion, nausea/vomiting, change in menstrual periods, trembling, unusual weight loss or gain

Occasional Side Effects: Clumsiness, constipation, dizziness, thrombocytopenia, liver problems, headache

Rare Side Effects: Drowsiness, rash, excitement, diplopia, nystagmus, pancreatitis

Contraindications: Liver problems

Antidotal Therapy: Supportive: may include emesis/gastric lavage; maintenance of urinary output; naloxone; hemodialysis; hemoperfusion

Disease States: Blood dyscrasias, organic brain disease, hypoalbuminemia, kidney problems, renal function impairment

Other Drugs: Alcohol, CNS depressants, heparin, thrombolytic agents, tricyclic antidepressants, phenothiazines, mefloquine, phenytoin, platelet aggregation inhibitors, barbiturates, primidone, carbamazepine, hepatotoxic medications

Lab Tests: Thyroid function, urine ketone, amino acid screening, metyrapone, serum bilirubin

Administrative Notes: Do not chew tablets or capsules

Dobutamine Hydrochloride

Trade Name(s): Dobutrex

Chemically Related To: Dopamine

Pregnancy Category: Adequate studies have not been done.

Medical Category: Cardiac stimulant

Accepted Indications: Cardiogenic shock

Mechanism of Action: Stimulates beta receptors of the heart

Half life: 2 min

Metabolism: Hepatic

Elimination: Renal

Research Notes: Onset of action, within 1–{endash}2 min; duration of action, several min

Adult Dosage: 2.5–{endash}15 m{mu}g/kg/min adjusted to individual patients

Child Dosage: 5–{endash}20 m{mu}g/kg/min adjusted to individual patients

Infant Dosage: Dosage not established

Dosage Forms: Injection: 12.5 mg/mL

By System: Cardiovascular

Warnings: Dosage must be adjusted to individual's requirements

Precautions: Monitor patient for blood pressure and cardiac output

Occasional Side Effects: Chest pain, shortness of breath, headache, nausea

Contraindications: Idiopathic hypertrophic subaortic stenosis

Antidotal Therapy: Because of short duration of action, no treatment other than withdrawal of drug is indicated

Disease States: Atrial fibrillation, hypertension, myocardial infarction, premature ventricular heartbeats, mechanical obstruction

Other Drugs: Beta-adrenergic blockers, hydrocarbon anesthetics, rauwolfia alkaloids, nitroprusside, guanethidine

Administrative Notes: Incompatible with alkaline solutions

Docusate Sodium

Trade Name(s): Afko-Lube, Colace, Diocto, Diosuccin, Pro-Sof

Chemically Related To: Sulfosuccinates

Pregnancy Category: C

Medical Category: Laxative

Accepted Indications: Constipation

Mechanism of Action: Stool softener–{endash}reduces surface film tension

Absorption/Distribution: Some absorption in duodenum and jejunum

Elimination: Bile, fecal

Research Notes: Softening usually occurs within 1–{endash}3 d; rectal dose works within 15 min

Adult Dosage: 50–{endash}360 mg/d

Child Dosage: 2–{endash}12 y: 50–{endash}150 mg/d

Infant Dosage: Less than 2 y: 25 mg/d

Dosage Forms: Capsules: 50 mg, 100 mg, 240 mg, and 250 mg; tablets: 50 mg and 100 mg; solution: 10 mg/mL and 50 mg/mL; syrup: 16.7 mg/5 mL and 20 mg/5 mL; rectal suspension: 283 mg/4 mL

By System: GI

Warnings: Overuse could lead to bowel movement dependency

Precautions: Do not use if symptoms of appendicitis are present

Occasional Side Effects: Intestinal cramping

Rare Side Effects: Rash

Contraindications: Appendicitis, rectal bleeding, CHF, diabetes mellitus, intestinal obstruction

Nutrition: Take liquid in milk or fruit juice

Other Drugs: Diuretics, potassium supplements, mineral oil, phenolphthalein, danthron

Lab Tests: Blood glucose concentrations, sodium potassium

Administrative Notes: Do not give within 2 h of other laxatives

Docusate Sodium/Ferrous Fumarate/Folic Acid/Multivitamins

Trade Name(s): Hemaferrin, Tabron Filmseal

Pregnancy Category: C

Medical Category: Hematinic

Accepted Indications: Anemia, vitamin/mineral supplement

Dosage Forms: Hemaferrin tablets: 25 mg/150 mg/0.4 mg/various amounts; Tabron Filmseal tablets: 50 mg/304.2 mg/1 mg/various amounts

Dopamine Hydrochloride

Trade Name(s): Intropin

Pregnancy Category: C

Medical Category: Vasopressor

Accepted Indications: Acute hypotension, cardiogenic shock, low cardiac output, CHF

Mechanism of Action: Stimulates adrenergic receptors

Absorption/Distribution: Widely distributed in the body

Half life: 2 min (plasma), 9 min (elimination)

Metabolism: Hepatic, renal

Elimination: Renal

Research Notes: Onset of action within 5 min; duration of action <10>

Adult Dosage: IV infusion: 0.5–{endash}10 m{mu}g/kg/min

Child Dosage: IV infusion: 5–{endash}20 m{mu}g/kg/min

Dosage Forms: Injection: 40 mg/mL, 80 mg/mL, and 160 mg/mL; dopamine HCl and dextrose injection: 800 m{mu}g/mL and 5% dextrose, 1.6 mg/mL and 5% dextrose, and 3.2 mg/mL and 5% dextrose

Frequent Side Effects: Headache, nausea, vomiting

Occasional Side Effects: Bradycardia, hypertension, angina, dyspnea, hypotension, tachycardia, ventricular arrhythmias, nervousness, restlessness

Rare Side Effects: Polyuria

Contraindications: Pheochromocytoma

Overdosage: Severe hypertension

Antidotal Therapy: May include reduction of rate of administration

Disease States: Acidosis, hypoxia, Raynaud's disease, asymmetric septal hypertrophy, tachyarrhythmias, ventricular fibrillation, hypovolemia, myocardial infarction, diabetes mellitus

Other Drugs: Doxapram, ergotamine, MAO inhibitors, levodopa, phenytoin, alpha-adrenergic blockers, hydrocarbon inhalation anesthetics, halothane, tricyclic antidepressants, beta-adrenergic blockers, cocaine, digitalis glycosides

Lab Tests: EKG, blood pressure

Doxacurium Chloride

Trade Name(s): Nuromax

Pregnancy Category: C

Medical Category: Neuromuscular blocking agent

Accepted Indications: Muscle relaxation for surgery

Unaccepted Indications: Prolonged mechanical ventilation

Mechanism of Action: Competes with acetylcholine

Half life: 86–{endash}123 min (elimination)

Elimination: Renal, biliary

Research Notes: Onset of action 4–{endash}5 min; duration of action varies by dosage and patient age

Adult Dosage: Initial: IV, 50–{endash}80 m{mu}g/kg; maintenance, IV, 5–{endash}10 m{mu}g/kg. Doses must be individualized

Elderly Dosage: May require lower dose

Child Dosage: Under 2 y: not established. 2–{endash}12 y: 3 m{mu}g/kg.

Infant Dosage: Not established

Dosage Forms: Injection: 1 mg/mL

Rare Side Effects: Double vision, fever, urticaria, cardiovascular effects, respiratory effects

Contraindications: Renal impairment

Antidotal Therapy: May include neostigmine, respiratory support

Disease States: Hypothermia, respiratory depression

Other Drugs: Procainamide, quinidine, calcium channel blockers, aminoglycosides, capreomycin, citrate-anticoagulated blood, lincomycin, polymyxins

Doxapram Hydrochloride

Trade Name(s): Dopram

Pregnancy Category: B

Medical Category: Respiratory stimulant

Accepted Indications: Respiratory depression

Unaccepted Indications: Respiratory depression caused by drug overdose

Mechanism of Action: Affects peripheral carotid chemoreceptors

IV: 1–{endash}2 min

Elimination: Fecal, renal

Research Notes: Onset of action 20–{endash}40 sec; duration of action 5–{endash}12 min

Adult Dosage: IV: 0.5 mg–{endash}1mg/kg, not to exceed 1.5 mg/kg as a single dose; may be repeated up to a maximum total dose of 2 mg/kg. IV infusion: initially, 5 mg/min, then reduce to 1–{endash}3 mg/min, not to exceed 4 mg/kg as total dose.

Elderly Dosage: May require lower dosage

Child Dosage: Under 12 y: not recommended

Infant Dosage: Under 12 y: not recommended

Dosage Forms: Injection: 20 mg/mL

Occasional Side Effects: Confusion, dizziness, increased sweating, nausea, vomiting, urination problems, diarrhea, headache, coughing

Rare Side Effects: Chest pain, hemolysis, thrombophlebitis, wheezing, trouble breathing

Contraindications: Cerebrovascular accidents, CHF, pulmonary disease

Overdosage: Convulsions, tachycardia, trembling

Disease States: Asthma, cerebral edema, cardiac disease, seizure disorders, hypertension, hyperthyroidism, pheochromocytoma, hepatic function impairment, renal function impairment

Other Drugs: Anesthetics, CNS stimulants, MAO inhibitors, vasopressors

Lab Tests: Deep tendon reflexes

Doxazosin Mesylate

Trade Name(s): Cardura

Chemically Related To: Prazosin

Pregnancy Category: B

Medical Category: Antihypertensive

Accepted Indications: Hypertension, benign prostatic hypertrophy

Mechanism of Action: Alpha-adrenergic blocker

Absorption/Distribution: Well absorbed from GI tract

Half life: 19–{endash}22 h

PO: 5–{endash}6 h

Metabolism: Hepatic

Elimination: Fecal/renal

Research Notes: Onset of action, 1–{endash}2 h; duration of action, 24 h

Adult Dosage: 1 mg once daily, before bedtime

Elderly Dosage: Greater hypotensive effect may indicate need for decreased dosage

Dosage Forms: Tablets: 1 mg, 2 mg, 4 mg, and 8 mg

By System: Cardiovascular

Warnings: May cause drowsiness and/or dizziness; do not take other medicines

Precautions: Use caution when driving and when arising suddenly

Frequent Side Effects: Dizziness, headache, tiredness

Occasional Side Effects: Arrhythmias, shortness of breath, tachycardia, swelling of lower extremities, nausea

Overdosage: Circulatory failure: hypotension

Antidotal Therapy: May include volume expanders; monitor fluids and electrolytes

Disease States: Liver and kidney problems

Nutrition: Control of diet and salt intake

Other Drugs: NSAIDs, estrogens, sympathomimetics, antihypertensives

Administrative Notes: May be used with a thiazide or beta-adrenergic blocker

Doxepin Hydrochloride

Trade Name(s): Sinequan

Chemically Related To: Tricyclic antidepressants

Pregnancy Category: Adequate studies have not been done

Medical Category: Antidepressant, antipanic agent, antineuralgic

Accepted Indications: Mental depression, panic disorder, neurogenic pain, headache (prophylaxis), pruritus

Mechanism of Action: Blocks reuptake of norepinephrine and serotonin

Absorption/Distribution: High protein binding; rapid absorption

Half life: 11–{endash}23 h

Metabolism: Hepatic

Elimination: Renal

Research Notes: Onset of action as an antidepressant, 2–{endash}3 w

Adult Dosage: 25 mg t.i.d. up to 150 mg/d for outpatients; 300 mg/d for hospitalized patients

Elderly Dosage: 25–{endash}50 mg/d

Child Dosage: Up to 12 y: not established

Infant Dosage: Not established

Dosage Forms: Capsules: 10 mg, 25 mg, 50 mg, and 75 mg; oral solution: 10 mg/mL

By System: CNS

Warnings: May cause drowsiness; avoid alcohol

Precautions: Caution if surgery required; avoid sun lamps, tanning booths, and prolonged exposure to the sun without sunscreen

Frequent Side Effects: Dizziness, drowsiness, headache, increased appetite, nausea, weight gain

Occasional Side Effects: Anticholinergic effects, arrhythmia, hypotension, nervousness, sexual function problems, diarrhea

Rare Side Effects: Agranulocytosis, allergic reaction, tinnitus, gum problems, seizures

Contraindications: Acute recovery period after myocardial infarction

Overdosage: Confusion, convulsion, drowsiness, enlarged pupils, hallucinations, dyspnea, vomiting

Antidotal Therapy: May include gastric lavage, activated charcoal, maintenance of body temperature and of respiratory and cardiac function, digitalization if necessary

Disease States: Asthma, bipolar disorders, blood disorders, glaucoma, liver and kidney problems, schizophrenia

Nutrition: May need additional riboflavin

Other Drugs: Sympathomimetics, MAO inhibitors, estrogens, antithyroid agents, CNS depressants, anticonvulsants

Lab Tests: Blood glucose concentrations, metyrapone, EKG

Administrative Notes: Oral solution must be diluted before being taken; when oral solution is dispensed, the manufacturer-provided graduated dropper should be included

Doxorubicin Hydrochloride

Trade Name(s): Adriamycin, Rubex

Chemically Related To: Anthracene

Pregnancy Category: Safety not established

Medical Category: Antineoplastic

Accepted Indications: Leukemia, neuroblastoma, Wilms' tumor, lymphomas, sarcomas, solid state carcinomas

Mechanism of Action: Interferes with RNA-DNA synthesis

Absorption/Distribution: Does not cross blood-brain barrier; not absorbed from GI tract

Half life: Alpha phase, 0.6 h; beta phase, 16.7 h

Metabolism: Hepatic

Elimination: Biliary, renal

Research Notes: 30 sec after IV administration, drug is present in liver, heart, and kidneys

Adult Dosage: Total cumulative dosage of 550 mg/m2

Elderly Dosage: Over 70 y: cardiotoxicity more frequent

Child Dosage: IV: 30 mg/m2/d on 3 successive days every 4 w

Infant Dosage: Up to 2 y: cardiotoxicity more frequent

Dosage Forms: Injection: 2 mg/mL; powder for injection: USP 10 mg, 20 mg, 50 mg, 100 mg, and 150 mg

Warnings: Do not inhale particles of drug or expose skin to drug

Precautions: Avoid immunizations; continue medication even if GI distress

Frequent Side Effects: Leukopenia, stomatitis, nausea and vomiting, loss of hair, reddish urine

Occasional Side Effects: Cardiotoxicity, tissue necrosis, GI ulceration, thrombocytopenia, diarrhea, postirradiation erythema

Rare Side Effects: Rash, wheezing

Disease States: Bone marrow depression, gout, heart or liver problems, chickenpox, herpes zoster

Nutrition: Need ample fluid intake

Other Drugs: Live virus vaccines, bone marrow depressants, probenecid, daunorubicin, sulfinpyrazone

Lab Tests: EKG; QRS reduction; uric acid concentrations

Administrative Notes: Do not mix with heparin, dexamethasone, fluorouracil, hydrocortisone, sodium succinate, aminophylline, or cephalothin

Doxycycline

Trade Name(s): Doryx, Doxy, Doxy-Caps, Monodox, Vibramycin, Vibra-Tabs

Chemically Related To: Tetracycline

Pregnancy Category: D

Medical Category: Antibacterial

Accepted Indications: Acne vulgaris, bronchitis, GI tract infections, pneumonia, Q fever, sinusitis, skin and soft tissue infection

Mechanism of Action: Inhibits bacterial protein synthesis at 50S ribosome

Absorption/Distribution: Well absorbed; achieves therapeutic concentrations in the eye; prostatic concentrations are approximately 60% of serum concentrations

Half life: 12–{endash}22 h

PO: 2–{endash}4 h

IV: 15–{endash}30 min

Metabolism: Hepatic

Elimination: Renal/fecal

Research Notes: GI secretion is an important route of excretion when doxycycline is administered to patients with impaired renal function

Adult Dosage: 50–{endash}300 mg/d

Elderly Dosage: Same as adult dose

Child Dosage: Up to 8 y: not recommended

Infant Dosage: Not recommended

Dosage Forms: For oral suspension: 25 mg/5 mL and 50 mg/5 mL; capsules: 50 mg and 100 mg; delayed-release capsules: 100 mg; tablets: 100 mg; injection: 100 mg (base) and 200 mg (base)

Warnings: Possible photosensitivity reactions

Precautions: Caution if dizziness, lightheadedness, or unsteadiness occurs

Frequent Side Effects: Discoloration of children's teeth, photosensitivity, CNS toxicity, GI disturbances (cramps)

Occasional Side Effects: Nephrogenic diabetes insipidus, pigmentation of skin and mucous membranes, fungal overgrowth, discolored tongue

Rare Side Effects: Benign intracranial hypertension, hepatotoxicity, pancreatitis

Disease States: Nephrogenic diabetes insipidus, hepatic and renal impairment

Other Drugs: Antacids, phenytoin, cholestyramine, oral contraceptives, penicillins, methoxyflurane, vitamin A

Lab Tests: BUN, bilirubin

Administrative Notes: Discard outdated or decomposed drug: it might be toxic

Dronabinol

Trade Name(s): Marinol

Chemically Related To: Cannabis

Scheduled Class: II

Abuse Potential: Slight

Pregnancy Category: C

Medical Category: Antiemetic

Accepted Indications: Cancer chemotherapy-induced nausea and vomiting

Mechanism of Action: Possible inhibition of vomiting control mechanism in the medulla oblongata

Absorption/Distribution: Present in breast milk

Half life: Alpha phase, 4 h; terminal phase, 25–{endash}36 h

PO: 2–{endash}4 h

Metabolism: Hepatic

Elimination: Fecal

Research Notes: May increase central sympathomimetic activity; may increase heart rate

Adult Dosage: 5–{endash}15 mg/m2

Elderly Dosage: 5–{endash}10 mg/m2

Child Dosage: Same as elderly dose

Infant Dosage: 5 mg/m2

Dosage Forms: Capsules: 2.5 mg, 5 mg, and 10 mg

By System: CNS subcortical nuclei

Warnings: Caution if dizziness, drowsiness, lightheadedness, or false sense of well-being occurs

Precautions: Avoid use of alcohol or other CNS depressants during therapy; be careful when arising suddenly from a supine, prone, or sitting position

Frequent Side Effects: Dizziness, drowsiness, loss of coordination

Occasional Side Effects: Tachycardia, changes in mood, confusion, delusions, hallucinations

Rare Side Effects: Blurred vision, dry mouth, orthostatic hypotension, restlessness

Overdosage: Change in mood, confusion, hallucinations, mental depression, nervousness, anxiety, tachycardia

Antidotal Therapy: May include supportive therapy, continuous blood pressure monitoring, treatment of hypotension or hypertension, cardiac monitoring

Disease States: Cardiac disorders, drug abuse, hypertension, manic or depressed state, schizophrenia

Other Drugs: Alcohol, other CNS depressants, apomorphine

Administrative Notes: Rebound of REM sleep has been reported after discontinuation of high doses

Droperidol/Fentanyl Citrate Droperidol/Fentanyl Citrate

Trade Name(s): Innovar Innovar

Scheduled Class: II II

Pregnancy Category: C C

Medical Category: Opioid analgesic, tranquilizer Opioid analgesic, tranquilizer

Accepted Indications: Anxiety and pain for surgical and diagnostic procedures, anesthetic premedication, anesthesia adjunct Anxiety and pain for surgical and diagnostic procedures, anesthetic premedication, anesthesia adjunct

Adult Dosage: Must be individualized Must be individualized

Elderly Dosage: May require lower dose May require lower dose

Child Dosage: 2 y and over: must be individualized 2 y and over: must be individualized

Infant Dosage: Under 2 y: safety and efficacy not established Under 2 y: safety and efficacy not established

Dosage Forms: Injection: 2.5 mg/0.05 mg/mL Injection: 2.5 mg/0.05 mg/mL

Frequent Side Effects: No incidence given for hypotension, muscle rigidity, respiratory depression, hypovolemia, bradycardia, apnea, tachycardia, dysphoria, postoperative drowsiness, restlessness, anxiety, extrapyramidal effects, hallucinations, mental depression, anaphylaxis, chills, dizziness, blurred vision, twitching, bronchospasm, laryngospasm, nausea, vomiting, diaphoresis, emergence delirium, increased blood pressure No incidence given for hypotension, muscle rigidity, respiratory depression, hypovolemia, bradycardia, apnea, tachycardia, dysphoria, postoperative drowsiness, restlessness, anxiety, extrapyramidal effects, hallucinations, mental depression, anaphylaxis, chills, dizziness, blurred vision, twitching, bronchospasm, laryngospasm, nausea, vomiting, diaphoresis, emergence delirium, increased blood pressure

Rare Side Effects: Neuroleptic malignant syndrome Neuroleptic malignant syndrome

Disease States: Head injury, brain tumor, cardiac dysrhythmia, anoxia, hypercarbia, electrolyte disturbances, alcohol withdrawal, COPD, respiratory problems, impaired hepatic function, impaired renal function, pheochromocytoma, bradyarrhythmia Head injury, brain tumor, cardiac dysrhythmia, anoxia, hypercarbia, electrolyte disturbances, alcohol withdrawal, COPD, respiratory problems, impaired hepatic function, impaired renal function, pheochromocytoma, bradyarrhythmia

Other Drugs: CNS depressants CNS depressants

Administrative Notes: Do not use if discolored or contains precipitate Do not use if discolored or contains precipitate

Dyclonine Hydrochloride

Trade Name(s): Dyclone, Sucrets

Pregnancy Category: C

Medical Category: Mucosal-local anesthetic

Accepted Indications: Esophageal pain, pharyngeal pain, laryngeal pain, mouth pain, tracheal pain, urinary tract pain, vaginal pain, gag reflex suppression, perioral lesions

Mechanism of Action: Blocks initiation of nerve impulses

Absorption/Distribution: Readily absorbed through mucous membranes

Research Notes: Onset of action up to 10 min, duration of action 30–{endash}60 min

Adult Dosage: Lozenges: 1 lozenge/2 h. Topical solution: topical, 40–{endash}200 mg, up to 300 mg per procedure.

Elderly Dosage: Same as adult dose

Child Dosage: Lozenges: 2 y and over: one 1.2 mg lozenge/2 h. Topical solution: not established.

Infant Dosage: Not established

Dosage Forms: Lozenges: 1.2 mg, 2 mg, and 3 mg. Topical solution: 0.5% and 1%.

Occasional Side Effects: Contact dermatitis, angioedema, burning, stinging, swelling

Contraindications: Infection at area of treatment, severe traumatized mucosa

Overdosage: CNS effects, methemoglobinemia

Dyphylline

Trade Name(s): Dilor, Dyflex, Lufyllin, Neothylline

Chemically Related To: Theophylline

Pregnancy Category: C

Medical Category: Bronchodilator

Accepted Indications: Asthma, bronchitis, emphysema, chronic obstructive pulmonary disease

Mechanism of Action: Relaxes bronchial smooth muscle

Absorption/Distribution: Rapidly absorbed from GI tract

Half life: 2–{endash}2.5 h

PO: Within 1 h

Metabolism: Hepatic

Elimination: Excreted primarily as unchanged drug in the urine

Adult Dosage: Elixir and tablets: up to 15 mg/kg q.i.d. Injection: IM 500 mg initially, followed by 250–{endash}500 mg q2–{endash}6h

Elderly Dosage: Lower dose may be required

Child Dosage: Must be individualized

Infant Dosage: Must be individualized

Dosage Forms: Elixir: 33.3 mg/5 mL and 53.3 mg/5 mL. Tablets: 200 mg and 400 mg. Injection: 250 mg/mL

Frequent Side Effects: Nausea, nervousness, restlessness

Occasional Side Effects: Gastric reflux

Contraindications: Gastritis, peptic ulcer, renal failure

Overdosage: Convulsions, arrhythmia, severe vomiting

Antidotal Therapy: May include supportive and symptomatic treatment

Disease States: Hypertension, renal disease

Other Drugs: Beta blockers, probenecid

Lab Tests: Pulmonary function measurements

Administrative Notes: Do not switch brands without physician's permission; not metabolized to theophylline

Dyphylline/Ephedrine/Guaifenesin/Phenobarbital

Trade Name(s): Lufyllin-EPG

Medical Category: Bronchodilator

Accepted Indications: Asthma

Adult Dosage: Elixir: 10–{endash}20 mL q.i.d.; tablets: 1–{endash}2 tablets q.i.d.

Dosage Forms: Elixir: 150 mg/24 mg/300 mg/24 mg; tablets: 100 mg/16 mg/200 mg/16 mg

Dyphylline/Guaifenesin

Trade Name(s): Bronkolate G, Dilor-G, Dyflex-G, Dyline-G.G., Lufyllin-GG

Medical Category: Bronchodilator

Accepted Indications: Asthma

Adult Dosage: Liquid: 5–{endash}10 mL t.i.d. or q.i.d.; elixir: 30 mL q.i.d.; tablets: 1–{endash}2 q.i.d.

Dosage Forms: Liquid 300 mg/300 mg; elixir: 100 mg/100 mg; tablets: 200 mg/200 mg

Echothiophate Iodide

Trade Name(s): Phospholine Iodide

Chemically Related To: Irreversible cholinesterase inhibitors

Pregnancy Category: C

Medical Category: Antiglaucoma agent, cyclostimulant, diagnostic aid

Accepted Indications: Glaucoma, esotropia (diagnosis and treatment)

Mechanism of Action: Cholinesterase inhibitor

Peak activity: Miosis: 2 h

Research Notes: Onset of miosis: less than 1 h; duration of miosis: up to 1 m

Adult Dosage: Antiglaucoma: to conjunctiva, 1 drop of 0.03%–{endash}0.25% solution 1–{endash}2 times daily

Elderly Dosage: Decreased concentration

Child Dosage: 2 y and over: same as adult dosage

Dosage Forms: For ophthalmic solution: 0.03%, 0.06%, 0.125%, and 0.25%

By System: Ocular

Warnings: For the eye only–{endash}decreases night vision

Precautions: Carry medical identification

Frequent Side Effects: Frequencies not given for stinging of eyes, headache, miosis

Rare Side Effects: Retinal detachment

Overdosage: Bradycardia, bronchospasm, hypotension, increased sweating, nausea/vomiting, diarrhea

Antidotal Therapy: May include atropine sulfate injection, IV pralidoxime CL, diazepam

Disease States: Glaucoma, peptic ulcer, myasthenia gravis, epilepsy, bronchial asthma, Down syndrome, hypertension

Other Drugs: Cholinesterase inhibitors, cocaine, succinylcholine, ophthalmic belladonna alkaloids, anticholinergics

Administrative Notes: Reconstituted solution is stable for 3–{endash}4 w at room temperature

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