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

RENAL FAILURE ACUTE ( 68 FDA reports)
BLOOD CREATININE INCREASED ( 40 FDA reports)
DYSARTHRIA ( 39 FDA reports)
VOMITING ( 38 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 33 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 32 FDA reports)
NAUSEA ( 31 FDA reports)
ENCEPHALOPATHY ( 29 FDA reports)
BLOOD UREA INCREASED ( 28 FDA reports)
SOMNOLENCE ( 27 FDA reports)
ANOREXIA ( 24 FDA reports)
DIZZINESS ( 24 FDA reports)
SPEECH DISORDER ( 24 FDA reports)
ABASIA ( 22 FDA reports)
MALAISE ( 22 FDA reports)
PYREXIA ( 22 FDA reports)
ASTHENIA ( 21 FDA reports)
DELIRIUM ( 20 FDA reports)
GAIT DISTURBANCE ( 20 FDA reports)
NERVOUS SYSTEM DISORDER ( 20 FDA reports)
HALLUCINATION ( 19 FDA reports)
DISORIENTATION ( 14 FDA reports)
HEADACHE ( 13 FDA reports)
MUSCULAR WEAKNESS ( 13 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
DEHYDRATION ( 10 FDA reports)
DYSLALIA ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
MELAENA ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
ANAEMIA ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
RESTLESSNESS ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
PSYCHIATRIC SYMPTOM ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
STUPOR ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MYOGLOBIN URINE PRESENT ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
ORAL HERPES ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 4 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
PAIN ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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