BIPRETERAX Side Effects

BIPRETERAX Safety Questions, BIPRETERAX Answers


More Here>>Side Effects - FDA Reports 2006-2008

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BIPRETERAX Safety Reports

Total BIPRETERAX reports: 1.
BIPRETERAX FDA safety alerts: No.
   Reported hospitalizations: 1.
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Consumer or non-health professional from FRANCE reported BIPRETERAX problem on Dec 04, 2006. Male patient, 69 years of age, weighting 277.8 lb, was diagnosed with erysipelas and was treated with BIPRETERAX. After drug was administered, patient experienced the following problems/side effects: accidental overdose, blood creatinine increased, blood potassium decreased, blood sodium decreased, fluid replacement, renal failure acute. BIPRETERAX dosage: unknown. During the same period patient was treated with VOLTAREN. 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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