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

RENAL FAILURE ( 7 FDA reports)
HYPOTENSION ( 6 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYST ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHIFT TO THE RIGHT ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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