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

DRUG INEFFECTIVE ( 9 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
BRADYCARDIA ( 7 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SINOATRIAL BLOCK ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
RENAL TUBULAR ACIDOSIS ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VIRAL MUTATION IDENTIFIED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD HIV RNA ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FAT ATROPHY ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HEREDITARY OPTIC ATROPHY ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV DISEASE PROGRESSION ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RALES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THIRST ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
URETHRITIS GONOCOCCAL ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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