warnings and cautions
WARNINGS AND PRECAUTIONS Keep out of reach of children.
FDA label d8bf9232-d752-43ee-b06e-f8aae7425269
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
- 7cb4b5f7-5c43-4be8-a41d-6e2fe6b6b5cf
- SPL ID
- d8bf9232-d752-43ee-b06e-f8aae7425269
- Version
- 5
- Effective date
- 2015-01-08
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:04:29
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 | d8bf9232-d752-43ee-b06e-f8aae7425269 | id | |
| spl set id | 7cb4b5f7-5c43-4be8-a41d-6e2fe6b6b5cf | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Post-marketing Experience The following adverse events have been identified during post-marketing use of Lymphomyosot® Injection Solution. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure • Allergic (hypersensitivity) skin reactions may occur in isolated cases. To report SUSPECTED ADVERSE REACTIONS, contact Heel Inc. at 1.800.920.9203 info@heelusa.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.