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

DIARRHOEA ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
VOMITING ( 11 FDA reports)
PYREXIA ( 10 FDA reports)
HYPOTENSION ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
DEHYDRATION ( 8 FDA reports)
DYSPNOEA ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
RASH ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MALAISE ( 6 FDA reports)
APHASIA ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HICCUPS ( 5 FDA reports)
INFECTION ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 5 FDA reports)
PANOPHTHALMITIS ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
COUGH ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ASCITES ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
FALL ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABULIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLADDER CALCULUS REMOVAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
ULCER ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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