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

HEADACHE ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AGITATION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SKIN CANCER METASTATIC ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
APATHY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use