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

HYPERTENSION ( 21 FDA reports)
DEPRESSION ( 19 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
DIZZINESS ( 16 FDA reports)
ANXIETY ( 14 FDA reports)
SINUSITIS ( 12 FDA reports)
CARDIOVASCULAR DISORDER ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
SYNCOPE ( 11 FDA reports)
ABDOMINAL WALL DISORDER ( 10 FDA reports)
ADVERSE DRUG REACTION ( 10 FDA reports)
CATARACT OPERATION ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 10 FDA reports)
DENTAL FISTULA ( 10 FDA reports)
DRY MOUTH ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
HORMONE LEVEL ABNORMAL ( 10 FDA reports)
INCISION SITE CELLULITIS ( 10 FDA reports)
JOINT ANKYLOSIS ( 10 FDA reports)
MYOSITIS ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
PERIODONTITIS ( 10 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 10 FDA reports)
STRESS URINARY INCONTINENCE ( 10 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 10 FDA reports)
TOOTH ABSCESS ( 10 FDA reports)
TRIGEMINAL NEURALGIA ( 10 FDA reports)
VERTIGO POSITIONAL ( 10 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
GASTRIC ULCER ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE ( 8 FDA reports)
NON-CARDIAC CHEST PAIN ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
FAILURE OF IMPLANT ( 7 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
RESORPTION BONE INCREASED ( 7 FDA reports)
SYNOVIAL CYST ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
ORGAN FAILURE ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
STRESS SYMPTOMS ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
INTRACARDIAC THROMBUS ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
FALL ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ALCOHOLISM ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INFECTION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
ABSCESS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SCAR ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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