FDA label e6f6abd4-53bb-46f4-a6f6-fe1d2ab91c90

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)

SPL set ID
7f2f057b-9afc-42ae-9d1d-1b1041d1360b
SPL ID
e6f6abd4-53bb-46f4-a6f6-fe1d2ab91c90
Version
2
Effective date
2006-09-14
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:50:06

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Excessive use of adrenergic aerosols is potentially dangerous. Fatalities have been reported following excessive use of metaproterenol sulfate as with other sympathomimetic inhalation preparations, and the exact cause is unknown. Cardiac arrest was noted in several cases. Paradoxical bronchoconstriction with repeated excessive administration has been reported with sympathomimetic agents. Patients should be advised to contact their physician in the event that they do not respond to their usual dose of sympathomimetic amine aerosol.

Adverse reactions cross-check#

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

adverse reactions

ADVERSE REACTIONS Adverse reactions are similar to those noted with other sympathomimetic agents. The most frequent adverse reactions to metaproterenol sulfate are nervousness and tachycardia which occur in about 1 in 7 patients, tremor which occurs in about 1 in 20 patients, and nausea which occurs in about 1 in 50 patients. Less frequent adverse reactions are hypertension, palpitations, vomiting and bad taste which occur in approximately 1 in 300 patients.

Reported adverse events (FAERS/openFDA)#

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