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GOITRE ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
VOMITING ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
FALL ( 1 FDA reports)
MANIA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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