ANGIOTENSIN II
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
- ANGIOTENSIN II
- Generic name
- ANGIOTENSIN II
- Manufacturer
- Gland Pharma Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 727d1102-fc46-46f8-b78e-fd13f0738fe4
- SPL ID
- db7a3372-cd0e-412e-a8e2-90b5fdcf3e3e
- Version
- 3
- Effective date
- 2025-06-04
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:38:53
| 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 | ANDA | 216966 | derived:openfda.application_number |
| application number | ANDA216966 | openfda.application_number | |
| brand name | ANGIOTENSIN II | openfda.brand_name | |
| generic name | ANGIOTENSIN II | openfda.generic_name | |
| manufacturer name | Gland Pharma Limited | openfda.manufacturer_name | |
| ndc | package | 68083-553-01 | openfda.package_ndc |
| ndc | product | 68083-553 | openfda.product_ndc |
| ndc11 | package | 68083055301 | derived:openfda.package_ndc |
| rxcui | 1999007 | openfda.rxcui | |
| spl id | db7a3372-cd0e-412e-a8e2-90b5fdcf3e3e | id | |
| spl set id | 727d1102-fc46-46f8-b78e-fd13f0738fe4 | set_id | |
| unii | M089EFU921 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS • There is a potential for venous and arterial thrombotic and thromboembolic events in patients who receive Angiotensin II. Use concurrent venous thromboembolism (VTE) prophylaxis. ( 5.1 , 6.1 ) 5.1 Risk for Thrombosis The safety of Angiotensin II was evaluated in 321 adults with septic or other distributive shock in a randomized, double-blind, placebo-controlled study, ATHOS-3. There was a higher incidence of arterial and venous thrombotic and thromboembolic events in patients who received Angiotensin II compared to placebo-treated patients in the ATHOS-3 study (13% vs. 5%). The major imbalance was in deep venous thromboses. Use concurrent venous thromboembolism (VTE) prophylaxis.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS The most common adverse reactions reported in greater than 10% in Angiotensin II treated patients were thromboembolic events. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Gland Pharma at (609)-250‐7990 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. ATHOS-3 The safety of Angiotensin II was evaluated in ATHOS-3 [see Warnings and Precautions (5.1) ] . Patients in ATHOS-3 were receiving other vasopressors in addition to Angiotensin II or placebo, which were titrated to effect on mean arterial pressure (MAP). Table 2 summarizes adverse reactions with an incidence of at least 4% among patients treated with Angiotensin II and with a rate of at least 1.5% higher with Angiotensin II than with placebo. Table 2: Adverse Reactions Occurring in ≥ 4% of Patients Treated with Angiotensin II and ≥ 1.5% More Often than in Placebo-treated Patients in ATHOS-3 A dverse Event Angiotensin II N= 163 Placebo N= 158 Thromboembolic events a 21 (12.9%) 8 (5.1%) Deep vein thrombosis 7 (4.3%) 0 (0.0%) Thrombocytopenia 16 (9.8%) 11 (7.0%) Tachycardia 14 (8.6%) 9 (5.7%) Fungal infection 10 (6.1%) 2 (1.3%) Delirium 9 (5.5%) 1 (0.6%) Acidosis 9 (5.5%) 1 (0.6%) Hyperglycemia 7 (4.3%) 4 (2.5%) Peripheral ischemia 7 (4.3%) 4 (2.5%) a Including arterial and venous thrombotic events
adverse reactions table
<table cellspacing="0" cellpadding="0" border="0" width="606"><colgroup><col width="34.7051056338028%"/><col width="34.0889084507042%"/><col width="31.205985915493%"/></colgroup><tbody><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="center" valign="top"><content styleCode="bold">A</content><content styleCode="bold">dverse Event</content> </td><td styleCode="Rrule" align="center" valign="top"><content styleCode="bold">Angiotensin II N=</content><content styleCode="bold">163</content> </td><td styleCode="Rrule" align="center" valign="top"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=</content><content styleCode="bold">158</content> </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top">Thromboembolic events<sup>a</sup> </td><td styleCode="Rrule" align="center" valign="top">21 (12.9%) </td><td styleCode="Rrule" align="center" valign="top">8 (5.1%) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top"> Deep vein thrombosis </td><td styleCode="Rrule" align="center" valign="top">7 (4.3%) </td><td styleCode="Rrule" align="center" valign="top">0 (0.0%) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top">Thrombocytopenia </td><td styleCode="Rrule" align="center" valign="top">16 (9.8%) </td><td styleCode="Rrule" align="center" valign="top"> 11 (7.0%) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top">Tachycardia </td><td styleCode="Rrule" align="center" valign="top">14 (8.6%) </td><td styleCode="Rrule" align="center" valign="top">9 (5.7%) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top">Fungal infection </td><td styleCode="Rrule" align="center" valign="top">10 (6.1%) </td><td styleCode="Rrule" align="center" valign="top">2 (1.3%) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top">Delirium </td><td styleCode="Rrule" align="center" valign="top">9 (5.5%) </td><td styleCode="Rrule" align="center" valign="top">1 (0.6%) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top">Acidosis </td><td styleCode="Rrule" align="center" valign="top">9 (5.5%) </td><td styleCode="Rrule" align="center" valign="top">1 (0.6%) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" align="justify" valign="top">Hyperglycemia </td><td styleCode="Rrule" align="center" valign="top">7 (4.3%) </td><td styleCode="Rrule" align="center" valign="top">4 (2.5%) </td></tr><tr><td styleCode="Lrule Rrule" align="justify" valign="top">Peripheral ischemia </td><td styleCode="Rrule" align="center" valign="top">7 (4.3%) </td><td styleCode="Rrule" align="center" valign="top">4 (2.5%) </td></tr></tbody></table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.