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

HYPERTENSION ( 8 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
DEATH ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
BLADDER NECK OPERATION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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