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

PNEUMONIA ( 8 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
COUGH ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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