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

BLOOD CREATININE INCREASED ( 10 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
DIZZINESS ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
BRONCHITIS ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
CHROMATURIA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
APHASIA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILE DUCT CANCER STAGE IV ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJURY ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
POISONING ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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