Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Target Concepts:
Gene/Protein
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Query: UMLS:C0017168 (
gastroesophageal reflux disease
)
11,783
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The case of a 3-week-old male infant is described. After receiving an iatrogenic overdose of metoclopramide (1.0 mg/kg every six hours) throughout a 36-hour period for the treatment of suspected
gastroesophageal reflux
, he became cyanotic, lethargic, and irritable, he fed poorly, and he had diarrhea and respiratory distress.
Methemoglobinemia
(20.5%) and reduced oxyhemoglobin saturation (79%) were identified. The patient had an excellent clinical response following a single IV dose of methylene blue. Subsequently, methemoglobin reductase activity was normal and there was no measurable hemoglobin M. The diagnosis of
methemoglobinemia
should be considered in any infant receiving large doses of metoclopramide who has clinical findings of cyanosis, ashen color, or a history of lethargy and/or motor restlessness.
...
PMID:Metoclopramide-induced methemoglobinemia. 340 65
With the removal of cisapride from the U.S. market, practitioners have increasingly used other medications, such as metoclopramide, to treat
gastroesophageal reflux
in pediatric patients. We describe the case of a neonate who developed
methemoglobinemia
after receiving metoclopramide at doses slightly above the recommended age-appropriate dosage. Health care providers should be aware of this potentially serious side effect in young infants who receive this medication.
...
PMID:Methemoglobinemia associated with metoclopramide therapy in a neonate. 2311 91