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

DIZZINESS ( 9 FDA reports)
DYSPNOEA ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
CHEST PAIN ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
AGITATION ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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