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

CONFUSIONAL STATE ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
DEHYDRATION ( 6 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
FALL ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGLOBULINAEMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
THIRST ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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