FDA label 06b8cf21-8604-4866-9efb-ece19d6cc0ab

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
7d8688b0-bb99-45f6-a4e4-de0236e5e22b
SPL ID
06b8cf21-8604-4866-9efb-ece19d6cc0ab
Version
2
Effective date
2004-05-21
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:24

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

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

adverse reactions

ADVERSE REACTIONS Adverse reactions are rare following oral administration of bethanechol chloride, but are more common following subcutaneous injection. Adverse reactions are more likely to occur when dosage is increased. The following adverse reactions have been observed: Body as a Whole: Malaise. Cardiovascular: Fall in blood pressure with reflex tachycardia, vasomotor response. Digestive: Colicky pain, abdominal cramps or discomfort, diarrhea, nausea and belching, salivation, and borborygmi. Skin: Flushing, producing a feeling of warmth; sensation of heat about the face; sweating. Respiratory: Asthmatic attacks and bronchial constriction. Nervous System: Headache. Renal: Urinary urgency. Special Senses: Lacrimation, miosis. Causal Relationship Unknown: The following adverse reactions have been reported, and a causal relationship to therapy with bethanechol chloride has not been established: Body as a Whole: Malaise. Nervous System: Seizures.

Reported adverse events (FAERS/openFDA)#

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