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ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
HEADACHE ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
FALL ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
TREMOR ( 4 FDA reports)
AMNESIA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ASCITES ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEAR ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYST ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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