FDA label 40855f1d-2dfd-4355-e054-00144ff8d46c
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
- 4be7615b-70a5-4912-b4a5-09656cab2187
- SPL ID
- 40855f1d-2dfd-4355-e054-00144ff8d46c
- Version
- 2
- Effective date
- 2016-11-04
- Source export date
- 2026-10-12
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:29:29
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 | 40855f1d-2dfd-4355-e054-00144ff8d46c | id | |
| spl set id | 4be7615b-70a5-4912-b4a5-09656cab2187 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Paradoxical Bronchospasm: Like other inhaled beta-adrenergic agonists, Xopenex Inhalation Solution can produce paradoxical bronchospasm, which may be life threatening. If paradoxical bronchospasm occurs, Xopenex Inhalation Solution should be discontinued immediately and alternative therapy instituted. It should be recognized that paradoxical bronchospasm, when associated with inhaled formulations, frequently occurs with the first use of a new canister or vial. Deterioration of Asthma: Asthma may deteriorate acutely over a period of hours or chronically over several days or longer. If the patient needs more doses of Xopenex Inhalation Solution than usual, this may be a marker of destabilization of asthma and requires reevaluation of the patient and treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, e.g., corticosteroids. Use of Anti-Inflammatory Agents: The use of beta-adrenergic agonist bronchodilators alone may not be adequate to control asthma in many patients. Early consideration should be given to adding anti-inflammatory agents, e.g., corticosteroids, to the therapeutic regimen. Cardiovascular Effects: Xopenex Inhalation Solution, like all other beta-adrenergic agonists, can produce a clinically significant cardiovascular effect in some patients, as measured by pulse rate, blood pressure, and/or symptoms. Although such effects are uncommon after administration of Xopenex Inhalation Solution at recommended doses, if they occur, the drug may need to be discontinued. In addition, beta-agonists have been reported to produce ECG changes, such as flattening of the T wave, prolongation of the QTc interval, and ST segment depression. The clinical significance of these findings is unknown. Therefore, Xopenex Inhalation Solution, like all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension. Do Not Exceed Recommended Dose: Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs in patients with asthma. The exact cause of death is unknown, but cardiac arrest following an unexpected development of a severe acute asthmatic crisis and subsequent hypoxia is suspected. Immediate Hypersensitivity Reactions: Immediate hypersensitivity reactions may occur after administration of racemic albuterol, as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, anaphylaxis, and oropharyngeal edema. The potential for hypersensitivity must be considered in the clinical evaluation of patients who experience immediate hypersensitivity reactions while receiving Xopenex Inhalation Solution.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions table
<table width="100%"> <col span="1" align="left" width="50.000%"/> <col span="1" align="left" width="50.000%"/> <tbody> <tr> <td>Body as a Whole: </td> <td>chills, pain, chest pain </td> </tr> <tr> <td>Cardiovascular System: </td> <td>ECG abnormal, ECG change, hypertension, hypotension, syncope </td> </tr> <tr> <td>Digestive System: </td> <td>diarrhea, dry mouth, dry throat, dyspepsia, gastroenteritis, nausea </td> </tr> <tr> <td>Hemic and Lymphatic System: </td> <td>lymphadenopathy </td> </tr> <tr> <td>Musculoskeletal System: </td> <td>leg cramps, myalgia </td> </tr> <tr> <td>Nervous System: </td> <td>anxiety, hypesthesia of the hand, insomnia, paresthesia, tremor </td> </tr> <tr> <td>Special Senses: </td> <td>eye itch </td> </tr> </tbody> </table>
adverse reactions table
<table ID="t5" width="100%"> <caption>Table 5: Most Frequently Reported Adverse Events (≥2% in Any Treatment Group) and Those Reported More Frequently Than in Placebo during the Double-Blind Period (ITT Population, 6-11 Years Old) </caption> <col span="1" align="left" width="25.888%"/> <col span="1" align="left" width="13.236%"/> <col span="1" align="left" width="15.219%"/> <col span="1" align="left" width="15.219%"/> <col span="1" align="left" width="15.219%"/> <col span="1" align="left" width="15.219%"/> <tbody> <tr> <td/> <td>Percent of Patients </td> </tr> <tr> <td>Body System Preferred Term </td> <td>Placebo (n=59) </td> <td>Xopenex 0.31 mg (n=66) </td> <td>Xopenex 0.63 mg (n=67) </td> <td>Racemic albuterol 1.25 mg (n=64) </td> <td>Racemic albuterol 2.5 mg (n=60) </td> </tr> <tr> <td>Body as a Whole </td> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td> Abdominal pain </td> <td>3.4 </td> <td>0 </td> <td>1.5 </td> <td>3.1 </td> <td>6.7 </td> </tr> <tr> <td> Accidental injury </td> <td>3.4 </td> <td>6.1 </td> <td>4.5 </td> <td>3.1 </td> <td>5.0 </td> </tr> <tr> <td> Asthenia </td> <td>0 </td> <td>3.0 </td> <td>3.0 </td> <td>1.6 </td> <td>1.7 </td> </tr> <tr> <td> Fever </td> <td>5.1 </td> <td>9.1 </td> <td>3.0 </td> <td>1.6 </td> <td>6.7 </td> </tr> <tr> <td> Headache </td> <td>8.5 </td> <td>7.6 </td> <td>11.9 </td> <td>9.4 </td> <td>3.3 </td> </tr> <tr> <td> Pain </td> <td>3.4 </td> <td>3.0 </td> <td>1.5 </td> <td>4.7 </td> <td>6.7 </td> </tr> <tr> <td> Viral Infection </td> <td>5.1 </td> <td>7.6 </td> <td>9.0 </td> <td>4.7 </td> <td>8.3 </td> </tr> <tr> <td/> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td>Digestive System </td> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td> Diarrhea </td> <td>0 </td> <td>1.5 </td> <td>6.0 </td> <td>1.6 </td> <td>0 </td> </tr> <tr> <td/> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td>Hemic and Lymphatic </td> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td> Lymphadenopathy </td> <td>0 </td> <td>3.0 </td> <td>0 </td> <td>1.6 </td> <td>0 </td> </tr> <tr> <td/> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td>Musculoskeletal System </td> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td> Myalgia </td> <td>0 </td> <td>0 </td> <td>1.5 </td> <td>1.6 </td> <td>3.3 </td> </tr> <tr> <td/> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td>Respiratory System </td> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td> Asthma </td> <td>5.1 </td> <td>9.1 </td> <td>9.0 </td> <td>6.3 </td> <td>10.0 </td> </tr> <tr> <td> Pharyngitis </td> <td>6.8 </td> <td>3.0 </td> <td>10.4 </td> <td>0 </td> <td>6.7 </td> </tr> <tr> <td> Rhinitis </td> <td>1.7 </td> <td>6.1 </td> <td>10.4 </td> <td>3.1 </td> <td>5.0 </td> </tr> <tr> <td/> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td>Skin and Appendages </td> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td> Eczema </td> <td>0 </td> <td>0 </td> <td>0 </td> <td>0 </td> <td>3.3 </td> </tr> <tr> <td> Rash </td> <td>0 </td> <td>0 </td> <td>7.5 </td> <td>1.6 </td> <td>0 </td> </tr> <tr> <td> Urticaria </td> <td>0 </td> <td>0 </td> <td>3.0 </td> <td>0 </td> <td>0 </td> </tr> <tr> <td/> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td>Special Senses </td> <td/> <td/> <td/> <td/> <td/> </tr> <tr> <td> Otitis Media </td> <td>1.7 </td> <td>0 </td> <td>0 </td> <td>0 </td> <td>3.3 </td> </tr> <tr> <td> <paragraph>Note: Subjects may have more than one adverse event per body system and preferred term. </paragraph> </td> </tr> </tbody> </table>
adverse reactions table
<table ID="t6" width="100%"> <caption>Table 6: Mean Changes from Baseline Heart Rate at 30 Minutes and Glucose and Potassium at 1 Hour after First Dose (Day 1) and Last Dose (Day 21) in Children 6-11 years old </caption> <col span="1" align="left" width="40.350%"/> <col span="1" align="left" width="20.600%"/> <col span="1" align="left" width="19.525%"/> <col span="1" align="left" width="19.525%"/> <tbody> <tr> <td>Treatment </td> <td>Mean Changes (Day 1) </td> </tr> <tr> <td>Heart Rate (bpm) </td> <td>Glucose (mg/dL) </td> <td>Potassium (mEq/L) </td> </tr> <tr> <td>Xopenex 0.31 mg, n=66 </td> <td>0.8 </td> <td>4.9 </td> <td>–0.31 </td> </tr> <tr> <td>Xopenex 0.63 mg, n=67 </td> <td>6.7 </td> <td>5.2 </td> <td>–0.36 </td> </tr> <tr> <td>Racemic albuterol 1.25 mg, n=64 </td> <td>6.4 </td> <td>8.0 </td> <td>–0.27 </td> </tr> <tr> <td>Racemic albuterol 2.5 mg, n=60 </td> <td>10.9 </td> <td>10.8 </td> <td>–0.56 </td> </tr> <tr> <td>Placebo, n=59 </td> <td>–1.8 </td> <td>0.6 </td> <td>–0.05 </td> </tr> <tr> <td/> <td>Mean Changes (Day 21) </td> </tr> <tr> <td>Treatment </td> <td>Heart Rate (bpm) </td> <td>Glucose (mg/dL) </td> <td>Potassium (mEq/L) </td> </tr> <tr> <td>Xopenex 0.31 mg, n= 60 </td> <td>0 </td> <td>2.6 </td> <td>–0.32 </td> </tr> <tr> <td>Xopenex 0.63 mg, n=66 </td> <td>3.8 </td> <td>5.8 </td> <td>–0.34 </td> </tr> <tr> <td>Racemic albuterol 1.25 mg, n= 62 </td> <td>5.8 </td> <td>1.7 </td> <td>–0.18 </td> </tr> <tr> <td>Racemic albuterol 2.5 mg, n= 54 </td> <td>5.7 </td> <td>11.8 </td> <td>–0.26 </td> </tr> <tr> <td>Placebo, n= 55 </td> <td>–1.7 </td> <td>1.1 </td> <td>–0.04 </td> </tr> </tbody> </table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.