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

DEPRESSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
PAIN ( 5 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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