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

PSEUDOMONAS INFECTION ( 6 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
LOBAR PNEUMONIA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
DRY GANGRENE ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLUCAGONOMA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BITE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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