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

ASTHMA ( 14 FDA reports)
NAUSEA ( 12 FDA reports)
VOMITING ( 11 FDA reports)
PNEUMONIA ( 10 FDA reports)
FATIGUE ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
COUGH ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
APHASIA ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DIPLOPIA ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
MUSCLE DISORDER ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
ORAL CANDIDIASIS ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
STRABISMUS ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
VOCAL CORD PARESIS ( 6 FDA reports)
DIZZINESS ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
CHEST PAIN ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RASH ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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