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

CONSTIPATION ( 18 FDA reports)
PAIN ( 13 FDA reports)
NAUSEA ( 12 FDA reports)
FATIGUE ( 11 FDA reports)
GASTRIC DISORDER ( 11 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
MULTIPLE MYELOMA ( 10 FDA reports)
NERVOUSNESS ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PSORIASIS ( 10 FDA reports)
CONTUSION ( 9 FDA reports)
FALL ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 8 FDA reports)
PERIORBITAL HAEMATOMA ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
COUGH ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
RASH ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
CATARACT ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
HOT FLUSH ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
PSORIATIC ARTHROPATHY ( 6 FDA reports)
TEMPORAL ARTERITIS ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
STRESS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
COLITIS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ULCER ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND ( 1 FDA reports)

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