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| (dan-troe-LEEN SO-dee-uhm) |
| Dantrium; Dantrium Intravenous |
| Class: Skeletal muscle relaxant/direct acting |
Action Affects contraction of muscle at site beyond myoneural junction and directly on muscle itself; believed to interfere with calcium release from sarcoplasmic reticulum. Affects CNS, causing drowsiness, dizziness and generalized weakness.
Indications Control of spasticity associated with spinal cord injury, stroke, cerebral palsy or multiple sclerosis; prophylaxis, treatment and postcrisis therapy of malignant hyperthermia. Unlabeled use(s): Management of exercise-induced muscle pain, neuroleptic malignant syndrome, heat stroke.
Contraindications Active hepatic disease; muscle spasm resulting from rheumatic disorders; where spasticity is used to sustain upright posture and balance in locomotion or to obtain or maintain increased function.
Chronic Spasticity
ADULT: PO Initial dose: 25 mg q day; increase at 4 to 7 day intervals to 25 mg bid to qid, up to max of 100 mg bid to qid if necessary. CHILDREN: PO Initial dose: 0.5 mg/kg bid; increase to 0.5 mg/kg tid to qid, then by increments of 0.5 mg/kg, up to 3 mg/kg bid to qid, if necessary. Maximum 100 mg qid.
Malignant Hyperthermia
ADULTS & CHILDREN: PREOPERATIVE PROPHYLAXIS: PO 4 to 8 mg/kg/day in 3 or 4 divided doses for 1 or 2 days prior to surgery with last dose given 3 to 4 hrs before surgery or IV 2.5 mg/kg » 1¼ hrs before anesthesia. Infused over 1 hr. May repeat during surgery, if needed. Treatment: IV 1 mg/kg by continuous rapid push; evaluate and repeat as needed until cumulative total dose is £ 10 mg/kg. POSTCRISIS FOLLOW-UP: PO 4 to 8 mg/kg/day in 4 divided doses for 1 to 3 days to prevent recurrence. If IV route must be utilized, start with ³ 1 mg/kg, as needed.
Clofibrate: Plasma protein binding of dantrolene reduced. Estrogens: Women receiving these may be at increased risk for hepatotoxicity. Verapamil: Hyperkalemia and myocardial depression possible. Warfarin: Plasma protein binding of dantrolene reduced.
Lab Test Interferences None well documented.
Due to oral administration except where otherwise indicated.
CV: Tachycardia; erratic blood pressure; phlebitis. CNS: Drowsiness; dizziness; weakness; general malaise; fatigue; speech disturbances; seizures; headache; lightheadedness; insomnia, mental depression or confusion; increased nervousness. DERM: Abnormal hair growth; acne-like rash; pruritus; urticaria (IV); eczematoid eruption; sweating; erythema (IV). EENT Visual disturbance, diplopia, alteration of taste. GI: Diarrhea; constipation; bleeding; anorexia; dysphagia; gastric irritation; abdominal cramps. GU Increased urinary frequency; hematuria; crystalluria; difficult erection; urinary incontinence; nocturia; dysuria; urinary retention. HEPA Hepatitis. RESP: Pleural effusion with pericarditis; pulmonary edema (IV). OTHER: Myalgia; backache; chills; fever; feeling of suffocation; excessive tearing; thrombophlebitis (IV).
Pregnancy: Category C (parenteral). Lactation: Do not use in nursing women. Children: Safety in children < 5 yr not established. Special risk patients: Use drug with caution in patients with impaired pulmonary function (especially COPD) or cardiac function. Hepatic effects: Fatal and nonfatal liver disorders may occur; use drug with caution in patients with pre-existing hepatic impairment and in females and patients > 35 yr. Long-term use: Safety and efficacy not established; use only if significant pain or disability is present or nursing care is reduced. Consider carcinogenicity risk and liver damage with long-term use. Discontinue therapy if no benefit within 45 days. Malignant hyperthermia: Supportive care should be foremost in treatment (ie, concurrent with dantrolene therapy). Extravasation: Because of the high pH of the IV formulation, prevent extravasation into the surrounding tissue. IV Dantrolene: IV dantrolene is also associated with the loss of grip strength and weakness in the legs.
| PATIENT CARE CONSIDERATIONS |
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