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

NAUSEA ( 13 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FALL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
RASH ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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