adverse reactions
ADVERSE REACTIONS Rash with generalized erythema, facial edema and fever has been reported in less than 1% of patients. A transient increase in blood pressure was seen in 8% of patients.
CERETEC
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
- Brand name
- CERETEC
- Generic name
- TECHNETIUM TC-99M EXAMETAZIME
- Manufacturer
- Medi-Physics Inc. dba GE Healthcare.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 3c1eca7e-57a0-4876-8ed6-cd655ef5e296
- SPL ID
- 87cca989-b750-4ca7-9b5a-6f00d0457c46
- Version
- 7
- Effective date
- 2024-01-10
- Source export date
- 2026-10-12
- 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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:12:54
| Harmonized routes |
|---|
| INTRAVENOUS |
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 |
|---|---|---|---|
| application applno | NDA | 019829 | derived:openfda.application_number |
| application number | NDA019829 | openfda.application_number | |
| brand name | CERETEC | openfda.brand_name | |
| generic name | TECHNETIUM TC-99M EXAMETAZIME | openfda.generic_name | |
| manufacturer name | Medi-Physics Inc. dba GE Healthcare. | openfda.manufacturer_name | |
| ndc | package | 17156-022-05 | openfda.package_ndc |
| ndc | product | 17156-022 | openfda.product_ndc |
| ndc11 | package | 17156002205 | derived:openfda.package_ndc |
| spl id | 87cca989-b750-4ca7-9b5a-6f00d0457c46 | id | |
| spl set id | 3c1eca7e-57a0-4876-8ed6-cd655ef5e296 | set_id | |
| unii | 3B744AG22N | openfda.unii |
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.