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

RETROPERITONEAL FIBROSIS ( 13 FDA reports)
DYSPNOEA ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
MELAENA ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
THROAT TIGHTNESS ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
DEATH ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
JOINT PROSTHESIS USER ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RENAL TUBULAR ATROPHY ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
URETERIC STENOSIS ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SOPOR ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COMA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MYOKYMIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KIDNEY MALROTATION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPATORY FINDING ABNORMAL ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SELECTIVE ABORTION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)

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