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HEPATITIS ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
SYPHILIS ( 3 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
RASH ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CELLULITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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