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GASTRIC DISORDER ( 16 FDA reports)
WHEEZING ( 16 FDA reports)
HYPERHIDROSIS ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
EYE IRRITATION ( 16 FDA reports)
DYSGEUSIA ( 16 FDA reports)
DRUG INEFFECTIVE ( 16 FDA reports)
COUGH ( 16 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 16 FDA reports)
CONDITION AGGRAVATED ( 16 FDA reports)
CHEST DISCOMFORT ( 16 FDA reports)
ORAL DISCOMFORT ( 16 FDA reports)
PAIN ( 12 FDA reports)
FOOD INTERACTION ( 12 FDA reports)
CROHN'S DISEASE ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
THROAT IRRITATION ( 12 FDA reports)
CONSTIPATION ( 12 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
BRONCHITIS ( 4 FDA reports)
MULTIPLE ALLERGIES ( 4 FDA reports)
MALAISE ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
ILEAL STENOSIS ( 3 FDA reports)
PERITONITIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
RASH ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
FALL ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)

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