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

DYSPNOEA ( 8 FDA reports)
ASTHENIA ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RASH ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GINGIVAL DISORDER ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BITE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER STAGE IV ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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