Albuterol Sulfate

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 (canonical bytes are SHA-256 checked before publication)

Brand name
Albuterol Sulfate
Generic name
ALBUTEROL SULFATE
Manufacturer
Proficient Rx LP
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
d3d2ab1e-8f91-4a4d-aa6b-5a57f59ad56b
SPL ID
621471a7-e06e-4d18-be4b-aca66c225a39
Version
5
Effective date
2022-11-01
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:23:56
Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS As with other inhaled beta-adrenergic agonists, albuterol sulfate inhalation solution can produce paradoxical bronchospasm, which can be life threatening. If it occurs, the preparation should be discontinued immediately and alternative therapy instituted. Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs and with the home use of nebulizers. It is, therefore, essential that the physician instruct the patient in the need for further evaluation, if his/her asthma becomes worse. In individual patients, any beta 2 -adrenergic agonist, including albuterol solution for inhalation, may have a clinically significant cardiac effect. Immediate hypersensitivity reactions may occur after administration of albuterol as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, and oropharyngeal edema.

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 2 matching rows.

adverse reactions

ADVERSE REACTIONS The results of clinical trials with albuterol sulfate inhalation solution in 135 patients showed the following side effects which were considered probably or possibly drug related: Central Nervous System: tremors (20%), dizziness (7%), nervousness (4%), headache (3%), insomnia (1%). Gastrointestinal: nausea (4%), dyspepsia (1%). Ear, Nose and Throat: pharyngitis (<1%), nasal congestion (1%). Cardiovascular: tachycardia (1%), hypertension (1%). Respiratory: bronchospasm (8%), cough (4%), bronchitis (4%), wheezing (1%). No clinically relevant laboratory abnormalities related to albuterol sulfate inhalation solution administration were determined in these studies. In comparing the adverse reactions reported for patients treated with albuterol sulfate inhalation solution with those of patients treated with isoproterenol during clinical trials of three months, the following moderate to severe reactions, as judged by the investigators, were reported. This table does not include mild reactions. Percent Incidence of Moderate to Severe Adverse Reactions Reaction Albuterol N=65 Isoproterenol N=65 Central Nervous System Tremors 10.7% 13.8% Headache 3.1% 1.5% Insomnia 3.1% 1.5% Cardiovascular Hypertension 3.1% 3.1% Arrhythmias 0% 3% *Palpitation 0% 22% Respiratory +Bronchospasm 15.4% 18% Cough 3.1% 5% Bronchitis 1.5% 5% Wheeze 1.5% 1.5% Sputum Increase 1.5% 1.5% Dyspnea 1.5% 1.5% Gastrointestinal Nausea 3.1% 0% Dyspepsia 1.5% 0% Systemic Malaise 1.5% 0% *The finding of no arrhythmias and no palpitations after albuterol administration in the clinical study should not be interpreted as indicating that these adverse effects cannot occur after the administration of inhaled albuterol. +In most cases of bronchospasm, this term was generally used to describe exacerbations in the underlying pulmonary disease. Cases of urticaria, angioedema, rash, bronchospasm, hoarseness, oropharyngeal edema, arrhythmias (including atrial fibrillations, supraventricular tachycardia, extrasystoles) have been reported after the use of albuterol sulfate inhalation solution.

adverse reactions table

<table ID="_RefID0EGBAE" width="100%"><caption> Percent Incidence of Moderate to Severe Adverse Reactions</caption><col width="33%"/><col width="33%"/><col width="33%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"><content styleCode="bold">Reaction </content></th><th align="center" styleCode="Rrule Botrule Lrule Toprule " valign="top"><content styleCode="bold">Albuterol</content> <content styleCode="bold">N=65 </content></th><th align="center" styleCode="Rrule Botrule Lrule Toprule " valign="top"><content styleCode="bold"> Isoproterenol</content> <content styleCode="bold">N=65</content></th></tr></thead><tbody><tr><td colspan="3" styleCode="Rrule Lrule Toprule " valign="top"><paragraph><content styleCode="bold">Central Nervous System</content></paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Tremors</paragraph></td><td valign="top"><paragraph>10.7%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>13.8%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Headache</paragraph></td><td valign="top"><paragraph>3.1%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>1.5%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Insomnia</paragraph></td><td valign="top"><paragraph>3.1%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>1.5%</paragraph></td></tr><tr><td colspan="3" styleCode="Rrule Lrule " valign="top"><paragraph><content styleCode="bold">Cardiovascular</content></paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Hypertension</paragraph></td><td valign="top"><paragraph>3.1%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>3.1%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Arrhythmias</paragraph></td><td valign="top"><paragraph>0%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>*Palpitation</paragraph></td><td valign="top"><paragraph>0%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>22%</paragraph></td></tr><tr><td colspan="3" styleCode="Rrule Lrule " valign="top"><paragraph><content styleCode="bold">Respiratory</content></paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>+Bronchospasm</paragraph></td><td valign="top"><paragraph>15.4%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>18%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Cough</paragraph></td><td valign="top"><paragraph>3.1%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>5%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Bronchitis</paragraph></td><td valign="top"><paragraph>1.5%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>5%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Wheeze</paragraph></td><td valign="top"><paragraph>1.5%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>1.5%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Sputum Increase</paragraph></td><td valign="top"><paragraph>1.5%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>1.5%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Dyspnea</paragraph></td><td valign="top"><paragraph>1.5%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>1.5%</paragraph></td></tr><tr><td colspan="3" styleCode="Rrule Lrule " valign="top"><paragraph><content styleCode="bold">Gastrointestinal</content></paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Nausea</paragraph></td><td valign="top"><paragraph>3.1%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>0%</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"><paragraph>Dyspepsia</paragraph></td><td valign="top"><paragraph>1.5%</paragraph></td><td styleCode="Rrule " valign="top"><paragraph>0%</paragraph></td></tr><tr><td colspan="3" styleCode="Rrule Lrule " valign="top"><paragraph><content styleCode="bold">Systemic</content></paragraph></td></tr><tr><td styleCode="Botrule Lrule " valign="top"><paragraph>Malaise</paragraph></td><td styleCode="Botrule " valign="top"><paragraph>1.5%</paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>0%</paragraph></td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.