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

DRUG INEFFECTIVE ( 11 FDA reports)
OFF LABEL USE ( 11 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
FATIGUE ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
COMA ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PUSTULAR PSORIASIS ( 4 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CATARACT ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOW SET EARS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ULCER ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BASOSQUAMOUS CARCINOMA ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PLACENTA PRAEVIA HAEMORRHAGE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use