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

DIARRHOEA ( 9 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
HYPERPARATHYROIDISM ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 5 FDA reports)
ATELECTASIS ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
MACROGLOSSIA ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
NASAL FLARING ( 2 FDA reports)
NITRITE URINE ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
RASH ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)

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