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

HEADACHE ( 12 FDA reports)
MYOCARDIAL ISCHAEMIA ( 11 FDA reports)
ACUTE PULMONARY OEDEMA ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
GASTRITIS ( 9 FDA reports)
HAEMATOCHEZIA ( 9 FDA reports)
HYPERAMMONAEMIA ( 9 FDA reports)
MALAISE ( 9 FDA reports)
ABDOMINAL DISCOMFORT ( 8 FDA reports)
ABDOMINAL TENDERNESS ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
BREATH SOUNDS ABNORMAL ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
CORONARY ARTERY STENOSIS ( 8 FDA reports)
COUGH ( 8 FDA reports)
CREPITATIONS ( 8 FDA reports)
GASTRIC ULCER ( 8 FDA reports)
HEPATITIS TOXIC ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
LUNG CONSOLIDATION ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
TROPONIN INCREASED ( 8 FDA reports)
NAUSEA ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
DEPRESSION ( 6 FDA reports)
CONVULSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FALL ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
COMA ( 3 FDA reports)
CRANIOPHARYNGIOMA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PAIN ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STARING ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN HAEMORRHAGE ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use