Please choose an event type to view the corresponding MedsFacts report:

HYPOTENSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PURPURA ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)

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