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

DIARRHOEA ( 12 FDA reports)
GROWTH RETARDATION ( 11 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
PYREXIA ( 6 FDA reports)
WHEEZING ( 5 FDA reports)
AGITATION ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
CRYING ( 5 FDA reports)
RESTLESSNESS ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
INTERCOSTAL RETRACTION ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
BREATH ODOUR ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
SLEEP TERROR ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROENTERITIS NOROVIRUS ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
LUNG DISORDER ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
RETINAL DYSTROPHY ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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