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

CONFUSIONAL STATE ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
FEELING HOT ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
PAIN ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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