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

CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
DIARRHOEA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
COUGH ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RASH ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THIRST ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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