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

CONFUSIONAL STATE ( 15 FDA reports)
RENAL FAILURE ( 13 FDA reports)
DIARRHOEA ( 11 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
FALL ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
MALAISE ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
COMA ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLATE ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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