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

BRONCHITIS ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
LUNG DISORDER ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
MALAISE ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
LIPIDS INCREASED ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
COUGH ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GOUT ( 5 FDA reports)
INFECTION ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
APICAL GRANULOMA ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
BRUXISM ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CHILLS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DIVERTICULUM INTESTINAL ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
FIBROMA ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GINGIVAL OEDEMA ( 4 FDA reports)
GINGIVAL SWELLING ( 4 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
MONARTHRITIS ( 4 FDA reports)
MORGANELLA INFECTION ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ORAL DISCHARGE ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
OTITIS EXTERNA ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
OVARIAN FAILURE ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PERCUSSION TEST ABNORMAL ( 4 FDA reports)
PERIODONTAL DISEASE ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
PRIMARY SEQUESTRUM ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SMEAR CERVIX ABNORMAL ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TOOTH FRACTURE ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SURGERY ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETHRAL DILATATION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RALES ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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