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Dantrolene Side Effects

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Dantrolene Safety Reports reported to FDA

Total Dantrolene reports: 4.
Dantrolene FDA safety alerts: No.
Reported deaths: 1    Reported hospitalizations: 2.
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Reported Dantrolene Side Effects: tenderness, pain in extremity, oedema peripheral, infusion related reaction, erythema, contusion, burning sensation, hepatic trauma, respiratory rate decreased, neuroleptic malignant syndrome, lethargy.
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Dantrolene Side Effects Report #5218780-4
Health Professional from UNITED STATES reported DANTROLENE problem on Jan 12, 2007. Female patient, 16 years of age, was diagnosed with analgesic effect and was treated with DANTROLENE. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, convulsion, cytolytic hepatitis, mucosal inflammation, nephropathy, renal failure, renal tubular disorder, thrombocytopenia. DANTROLENE dosage: unknown. During the same period patient was treated with METHOTREXATE, ONDANSETRON, METHYLPREDNISOLONE, NALBUPHINE. Patient recovered.

Dantrolene Side Effects Report #5145959-2
DANTROLENE problem was reported by a Physician from UNITED STATES on Nov 06, 2006. Male patient, 44 years of age, weighting 300.0 lb, was diagnosed with neuroleptic malignant syndrome, hypertension, schizoaffective disorder and was treated with DANTROLENE. After drug was administered, patient experienced the following problems/side effects: agitation, blood pressure abnormal, brain damage, cardiac arrest, disease recurrence, job dissatisfaction, lethargy, neuroleptic malignant syndrome, respiratory rate decreased. DANTROLENE dosage: 116 MG IV Q 6HRS. During the same period patient was treated with NORVASC, CLOZAPINE, ATENOLOL, CLONAZEPAM, GLIPIZIDE, BROMOCRIPTIN, INSULIN. Patient died on 09/01/2006.

Dantrolene Side Effects Report #5151276-7
Pharmacist from UNITED STATES reported DANTROLENE problem on Nov 13, 2006. Female patient, weighting 130.0 lb, was diagnosed with muscle spasticity and was treated with DANTROLENE. After drug was administered, patient experienced the following problems/side effects: hepatic trauma. DANTROLENE dosage: 50 MG 4 TIMES DAILY ORAL. Patient was hospitalized. Patient recovered.

Dantrolene Side Effects Report #5465358-3
DANTROLENE problem was reported by a Pharmacist from UNITED STATES on Sept 20, 2007. Female patient, 40 years of age, weighting 172.0 lb, was diagnosed with hyperthermia malignant and was treated with DANTROLENE. After drug was administered, patient experienced the following problems/side effects: burning sensation, contusion, erythema, infusion related reaction, oedema peripheral, pain in extremity, tenderness. DANTROLENE dosage: 200MG 1 DOSE IV 53 MG EVERY 4 HOURS IV. Patient was hospitalized. Patient recovered.


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ALABAMA
ALASKA
AMERICAN SAMOA
ARIZONA
ARKANSAS
CALIFORNIA
COLORADO
CONNECTICUT
DELAWARE
DISTRICT OF COLUMBIA
FEDERATED STATES OF MICRONESIA
FLORIDA
GEORGIA
GUAM
HAWAII
IDAHO
ILLINOIS
INDIANA
IOWA
KANSAS
KENTUCKY
LOUISIANA
MAINE
MARSHALL ISLANDS
MARYLAND
MASSACHUSETTS
MICHIGAN
MINNESOTA
MISSISSIPPI
MISSOURI
MONTANA
NEBRASKA
NEVADA
NEW HAMPSHIRE
NEW JERSEY
NEW MEXICO
NEW YORK
NORTH CAROLINA
NORTH DAKOTA
NORTHERN MARIANA ISLANDS
OHIO
OKLAHOMA
OREGON
PALAU
PENNSYLVANIA
PUERTO RICO
RHODE ISLAND
SOUTH CAROLINA
SOUTH DAKOTA
TENNESSEE
TEXAS
UTAH
VERMONT
VIRGIN ISLANDS
VIRGINIA
WASHINGTON
WEST VIRGINIA
WISCONSIN
WYOMING
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