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

DRUG INEFFECTIVE ( 7 FDA reports)
NAUSEA ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
DIARRHOEA ( 5 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
STUPOR ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMALL INTESTINE CARCINOMA STAGE IV ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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