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

CONDITION AGGRAVATED ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
DYSPNOEA ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SHOCK ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THIRST ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONSILLITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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