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

CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
COMPLEMENT FACTOR C1 DECREASED ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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