FDA label 4ebb446e-0ca4-44cb-a835-d3f989e8de88

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: 767aa369-d356-46d4-b9dc-db5342c4d32c
SPL ID: 4ebb446e-0ca4-44cb-a835-d3f989e8de88
Version: 3
Effective date: 2016-05-18
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 05:50:26

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		4ebb446e-0ca4-44cb-a835-d3f989e8de88	id
spl set id		767aa369-d356-46d4-b9dc-db5342c4d32c	set_id

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings FEDERAL LAW PROHIBITS DISPENISNG WITHOUT A PRESCRIPTION.

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: The most severe adverse effectis hyperkalemia which may casue cardiac arrhytmias, heart block, and fall in blood pressure. Flaccid paralysis, mental confussion, lislessness, paresthesias of the extremities, and weakness of the legs may be present. Nausea, vomiting, and diarreha are best avoided by dilutingthe preparation as specified in DOSAGE AND ADMINISTRATION, and taking with food.

Reported adverse events (FAERS/openFDA)#

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