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

ASTHENIA ( 14 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
ANOREXIA ( 12 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 12 FDA reports)
FIBROMYALGIA ( 12 FDA reports)
TENDONITIS ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 12 FDA reports)
LARYNGITIS ( 12 FDA reports)
DERMATOMYOSITIS ( 12 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
VOCAL CORD POLYP ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
PAIN ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
ANXIETY ( 8 FDA reports)
INJURY ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
POLYP ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
CARDIOLIPIN ANTIBODY ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
FALL ( 3 FDA reports)
INFECTION ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
APHONIA ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
FEAR ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NODULE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
COUGH ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
RASH ( 1 FDA reports)
MALAISE ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)

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