FDA label 4fbba89e-f8f7-47fa-a395-2eb2a1e049ef
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- SPL set ID
- 06079a6b-4710-4e89-b9dc-4a886223d175
- SPL ID
- 4fbba89e-f8f7-47fa-a395-2eb2a1e049ef
- Version
- 3
- Effective date
- 2015-07-14
- Source export date
- 2026-10-12
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:26:00
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| spl id | 4fbba89e-f8f7-47fa-a395-2eb2a1e049ef | id | |
| spl set id | 06079a6b-4710-4e89-b9dc-4a886223d175 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS During the double-blind, placebo-controlled clinical trial, six cases of necrotizing enterocolitis developed among the 85 infants studied (caffeine=46, placebo=39), with three cases resulting in death. Five of the six patients with necrotizing enterocolitis were randomized to or had been exposed to caffeine citrate. Reports in the published literature have raised a question regarding the possible association between the use of methylxanthines and development of necrotizing enterocolitis, although a causal relationship between methylxanthine use and necrotizing enterocolitis has not been established. Therefore, as with all preterm infants, patients being treated with caffeine citrate should be carefully monitored for the development of necrotizing enterocolitis.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Overall, the reported number of adverse events in the double-blind period of the controlled trial was similar for the caffeine citrate and placebo groups. The following table shows adverse events that occurred in the double-blind period of the controlled trial and that were more frequent in caffeine citrate treated patients than placebo. ADVERSE EVENTS THAT OCCURRED MORE FREQUENTLY IN CAFFEINE CITRATE TREATED PATIENTS THAN PLACEBO DURING DOUBLE-BLIND THERAPY Adverse Event (AE) Caffeine Citrate N=46 n (%) Placebo N=39 n (%) BODY AS A WHOLE Accidental Injury Feeding Intolerance Sepsis 1 (2.2) 4 (8.7) 2 (4.3) 0 (0) 2 (5.1) 0 (0) CARDIOVASCULAR SYSTEM Hemorrhage 1 (2.2) 0 (0) DIGESTIVE SYSTEM Necrotizing Enterocolitis Gastritis Gastrointestinal Hemorrhage 2 (4.3) 1 (2.2) 1 (2.2) 1 (2.6) 0 (0) 0 (0) HEMIC AND LYMPHATIC SYSTEM Disseminated Intravascular Coagulation 1 (2.2) 0 (0) METABOLIC AND NUTRITIVE DISORDERS Acidosis Healing Abnormal 1 (2.2) 1 (2.2) 0 (0) 0 (0) NERVOUS SYSTEM Cerebral Hemorrhage 1 (2.2) 0 (0) RESPIRATORY SYSTEM Dyspnea Lung Edema 1 (2.2) 1 (2.2) 0 (0) 0 (0) SKIN AND APPENDAGES Dry Skin Rash Skin Breakdown 1 (2.2) 4 (8.7) 1 (2.2) 0 (0) 3 (7.7) 0 (0) SPECIAL SENSES Retinopathy of Prematurity 1 (2.2) 0 (0) UROGENITAL SYSTEM Kidney Failure 1 (2.2) 0 (0) In addition to the cases above, three cases of necrotizing enterocolitis were diagnosed in patients receiving caffeine citrate during the open-label phase of the study. Three of the infants who developed necrotizing enterocolitis during the trial died. All had been exposed to caffeine. Two were randomized to caffeine, and one placebo patient was "rescued" with open-label caffeine for uncontrolled apnea. Adverse events described in the published literature include: central nervous system stimulation (i.e., irritability, restlessness, jitteriness), cardiovascular effects (i.e., tachycardia, increased left ventricular output, and increased stroke volume), gastrointestinal effects (i.e., increased gastric aspirate, gastrointestinal intolerance), alterations in serum glucose (hypoglycemia and hyperglycemia) and renal effects (increased urine flow rate, increased creatinine clearance, and increased sodium and calcium excretion). Published long-term follow-up studies have not shown caffeine to adversely affect neurological development or growth parameters.
adverse reactions table
<table ID="_RefID0ETBAE"> <caption>ADVERSE EVENTS THAT OCCURRED MORE FREQUENTLY IN CAFFEINE CITRATE TREATED PATIENTS THAN PLACEBO DURING DOUBLE-BLIND THERAPY</caption> <col width="60%"/> <col width="20%"/> <col width="20%"/> <thead> <tr> <th styleCode="Botrule Lrule Toprule "> <content styleCode="bold">Adverse Event (AE)</content> </th> <th styleCode="Botrule Lrule Toprule "> <content styleCode="bold">Caffeine Citrate </content> <content styleCode="bold">N=46</content> <content styleCode="bold">n (%)</content> </th> <th styleCode="Rrule Botrule Lrule Toprule "> <content styleCode="bold">Placebo </content> <content styleCode="bold">N=39</content> <content styleCode="bold">n (%)</content> </th> </tr> </thead> <tbody> <tr> <td styleCode="Lrule Toprule " valign="top"> <paragraph>BODY AS A WHOLE</paragraph> </td> <td styleCode="Lrule Toprule " valign="top"/> <td styleCode="Rrule Lrule Toprule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Accidental Injury Feeding Intolerance Sepsis</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2) 4 (8.7) 2 (4.3)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0) 2 (5.1) 0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>CARDIOVASCULAR SYSTEM</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Hemorrhage</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>DIGESTIVE SYSTEM</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Necrotizing Enterocolitis Gastritis Gastrointestinal Hemorrhage</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>2 (4.3) 1 (2.2) 1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>1 (2.6) 0 (0) 0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>HEMIC AND LYMPHATIC SYSTEM</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Disseminated Intravascular Coagulation</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>METABOLIC AND NUTRITIVE DISORDERS</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Acidosis Healing Abnormal</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2) 1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0) 0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>NERVOUS SYSTEM</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Cerebral Hemorrhage</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>RESPIRATORY SYSTEM</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Dyspnea Lung Edema</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2) 1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0) 0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>SKIN AND APPENDAGES</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Dry Skin Rash Skin Breakdown</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2) 4 (8.7) 1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0) 3 (7.7) 0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>SPECIAL SENSES</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Lrule Botrule " valign="top"> <paragraph> Retinopathy of Prematurity</paragraph> </td> <td styleCode="Lrule Botrule " valign="top"> <paragraph>1 (2.2)</paragraph> </td> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>0 (0)</paragraph> </td> </tr> <tr> <td styleCode="Lrule " valign="top"> <paragraph>UROGENITAL SYSTEM</paragraph> </td> <td styleCode="Lrule " valign="top"/> <td styleCode="Rrule Lrule " valign="top"/> </tr> <tr> <td styleCode="Botrule Lrule " valign="top"> <paragraph> Kidney Failure</paragraph> </td> <td styleCode="Botrule Lrule " valign="top"> <paragraph>1 (2.2)</paragraph> </td> <td styleCode="Rrule Botrule Lrule " valign="top"> <paragraph>0 (0)</paragraph> </td> </tr> </tbody> </table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.