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

RENAL FAILURE ( 3 FDA reports)
COMA ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
RASH ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)

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