Giapreza

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)

Brand name
Giapreza
Generic name
ANGIOTENSIN II
Manufacturer
La Jolla Pharmaceutical Company
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
c265d69a-3efe-4107-9a9e-e6fd3d531c48
SPL ID
2c555078-770d-43d9-93e5-40e4cf5a4acf
Version
18
Effective date
2026-07-22
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:42
Harmonized routes table
Harmonized routes
INTRAVENOUS

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings and cautions

5. WARNINGS AND PRECAUTIONS There is a potential for venous and arterial thrombotic and thromboembolic events in patients who receive GIAPREZA. Use concurrent venous thromboembolism (VTE) prophylaxis. ( 5.1 , 6.1 ) 5.1 Risk for Thrombosis The safety of GIAPREZA 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 GIAPREZA 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#

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Adverse reactions sections page 1 of 1 · 2 matching rows.

adverse reactions

6. ADVERSE REACTIONS The most common adverse reactions reported in greater than 10% of GIAPREZA treated patients were thromboembolic events. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact La Jolla Pharmaceutical Company at 1-800-651-3861 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 GIAPREZA was evaluated in ATHOS-3 [see Warnings and Precautions(5.1) ] . Patients in ATHOS-3 were receiving other vasopressors in addition to GIAPREZA or placebo, which were titrated to effect on mean arterial pressure (MAP). Table 1 summarizes adverse reactions with an incidence of at least 4% among patients treated with GIAPREZA and with a rate of at least 1.5% higher with GIAPREZA than with placebo. Table 1: Adverse Reactions Occurring in ≥ 4% of Patients Treated with GIAPREZA and ≥ 1.5% More Often than in Placebo-treated Patients in ATHOS-3 Adverse Event GIAPREZA N=163 Placebo N=158 Thromboembolic events Including arterial and venous thrombotic events 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%)

adverse reactions table

<table width="75%"><caption>Table 1: Adverse Reactions Occurring in &#x2265; 4% of Patients Treated with GIAPREZA and &#x2265; 1.5% More Often than in Placebo-treated Patients in ATHOS-3</caption><colgroup><col align="left" valign="top" width="34%"/><col align="center" valign="top" width="33%"/><col align="center" valign="top" width="33%"/></colgroup><thead><tr><th styleCode="Lrule Rrule">Adverse Event</th><th styleCode="Rrule">GIAPREZA N=163</th><th styleCode="Rrule">Placebo N=158</th></tr></thead><tbody><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Thromboembolic events <footnote ID="K802">Including arterial and venous thrombotic events</footnote></td><td styleCode="Rrule">21 (12.9%)</td><td styleCode="Rrule">8 (5.1%)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule"> Deep vein thrombosis</td><td styleCode="Rrule">7 (4.3%)</td><td styleCode="Rrule">0 (0.0%)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Thrombocytopenia</td><td styleCode="Rrule">16 (9.8%)</td><td styleCode="Rrule">11 (7.0%)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Tachycardia</td><td styleCode="Rrule">14 (8.6%)</td><td styleCode="Rrule">9 (5.7%)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Fungal infection</td><td styleCode="Rrule">10 (6.1%)</td><td styleCode="Rrule">2 (1.3%)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Delirium</td><td styleCode="Rrule">9 (5.5%)</td><td styleCode="Rrule">1 (0.6%)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Acidosis</td><td styleCode="Rrule">9 (5.5%)</td><td styleCode="Rrule">1 (0.6%)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Hyperglycemia</td><td styleCode="Rrule">7 (4.3%)</td><td styleCode="Rrule">4 (2.5%)</td></tr><tr><td styleCode="Lrule Rrule">Peripheral ischemia</td><td styleCode="Rrule">7 (4.3%)</td><td styleCode="Rrule">4 (2.5%)</td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

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