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

DRUG ADMINISTRATION ERROR ( 16 FDA reports)
HAEMOLYTIC ANAEMIA ( 16 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
SYNCOPE ( 10 FDA reports)
MALAISE ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
PAIN ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
CHILLS ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
VIITH NERVE PARALYSIS ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
HAEMATOMA INFECTION ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
SERRATIA BACTERAEMIA ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CRYING ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
FALL ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOREPINEPHRINE DECREASED ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)

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