FDA label 2b4bac3e-4a5a-3675-e063-6294a90afee7

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
689750b7-8e51-47d9-a428-078f3f6c9dec
SPL ID
2b4bac3e-4a5a-3675-e063-6294a90afee7
Version
5
Effective date
2025-01-09
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:33:27

Boxed warning cross-check#

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boxed warning

WARNING: ABUSE AND DEPENDENCE CNS stimulants, including cocaine hydrochloride, have a high potential for abuse and dependence [see Warnings and Precautions (5.1) . WARNING: ABUSE AND DEPENDENCE See full prescribing information for complete boxed warning. CNS stimulants, including cocaine hydrochloride, have a high potential for abuse and dependence. ( 5.1 )

Warnings cross-check#

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warnings and cautions

5 WARNINGS AND PRECAUTIONS Seizures : GOPRELTO may lower the convulsive threshold. Monitor patients for development of seizures. ( 5.2 ) Blood Pressure and Heart Rate Increases : Monitor vital signs, including heart rate and rhythm, in patients after receiving GOPRELTO. Avoid use of GOPRELTO in patients with a recent or active history of uncontrolled hypertension, unstable angina, myocardial infarction, coronary artery disease, or congestive heart failure. ( 5.3 ) 5.1 Potential for Abuse and Dependence Central nervous system (CNS) stimulants, including cocaine hydrochloride, have a high potential for abuse and dependence [see Drug Abuse and Dependence (9.2 , 9.3) ] . 5.2 Seizures It has been reported in the literature that cocaine hydrochloride may lower the convulsive threshold. The risk may be higher in patients with a history of seizures or in patients with prior electroencephalogram (EEG) abnormalities without seizures, but has been reported in patients with no prior history or EEG evidence of seizures. Monitor patients for development of seizures. 5.3 Blood Pressure and Heart Rate Increases As reported in the literature, cocaine hydrochloride causes an increase in observed blood pressure and heart rate. In the Phase 3 clinical study with GOPRELTO, increases in blood pressure and heart rate were observed for 60 minutes or longer following pledget removal. Monitor for vital sign changes, including heart rate and rhythm, after administration of GOPRELTO. Avoid use of GOPRELTO in patients with a recent or active history of uncontrolled hypertension, unstable angina, myocardial infarction, coronary artery disease, or congestive heart failure. Avoid use of additional vasoconstrictor agents such as epinephrine or phenylephrine with GOPRELTO. If concomitant use is unavoidable, prolonged vital sign and ECG monitoring may be required [see Drug Interactions (7) ]. 5.4 Toxicology Screening The cocaine hydrochloride in GOPRELTO may be detected in plasma for up to one week after administration. Cocaine hydrochloride and its metabolites may be detected in urine toxicology screening for longer than one week after administration.

Adverse reactions cross-check#

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adverse reactions

6 ADVERSE REACTIONS The most common adverse reactions (>0.5%) occurring in patients treated with GOPRELTO (cocaine hydrochloride) nasal solution 4% were headache and epistaxis. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Pharm-Olam at 1-866-511-6754 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trial 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. GOPRELTO has been evaluated in four Phase 1 studies and one Phase 3 study, which included 647 adult subjects who received a single topical intranasal 160 mg dose (four pledgets), of GOPRELTO. The randomized, double-blind, controlled Phase 3 study was conducted in adult patients undergoing diagnostic procedures and surgeries on or through the mucous membranes of the nasal cavities, of which 278 received GOPRELTO (4% solution), 275 received cocaine hydrochloride solution 8%, and 95 received placebo. Safety was evaluated for up to 7 days after dosing. The most commonly reported adverse reactions (>1 patient) to occur in the Phase 3 study with GOPRELTO (4% solution) were headache and epistaxis. Two adverse reactions of headache were severe (Table 1). No premature discontinuations due to an adverse event, serious adverse events, or deaths were reported in the Phase 3 clinical study. Table 1: Common Adverse Reactions with GOPRELTO in >1 Patient System Organ Class / Preferred Term GOPRELTO 4% (N=278) Cocaine Hydrochloride Solution 8% (N=275) Placebo (N=95) Nervous System Disorders Headache 7 (3%) 4 (2%) 1 (1%) Respiratory, Thoracic, and Mediastinal Disorders Epistaxis 3 (1%) 2 (1%) 0 Psychiatric Disorders Anxiety 0 2 (1%) 0

adverse reactions table

<table width="80%" ID="table1"><caption>Table 1: Common Adverse Reactions with GOPRELTO in &gt;1 Patient</caption><col width="28%" align="left" valign="top"/><col width="25%" align="center" valign="top"/><col width="26%" align="center" valign="top"/><col width="21%" align="center" valign="top"/><thead><tr><th align="center" styleCode="Lrule Rrule" valign="middle">System Organ Class / Preferred Term</th><th align="center" styleCode="Rrule" valign="middle">GOPRELTO 4% (N=278) </th><th align="center" styleCode="Rrule" valign="middle">Cocaine Hydrochloride Solution 8% (N=275) </th><th align="center" styleCode="Rrule" valign="middle">Placebo (N=95) </th></tr></thead><tbody><tr styleCode="Botrule"><td colspan="4" styleCode="Lrule Rrule"><content styleCode="bold">Nervous System Disorders</content></td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule"> Headache</td><td styleCode="Rrule">7 (3%)</td><td styleCode="Rrule">4 (2%)</td><td styleCode="Rrule">1 (1%)</td></tr><tr styleCode="Botrule"><td colspan="4" styleCode="Lrule Rrule"><content styleCode="bold">Respiratory, Thoracic, and Mediastinal Disorders</content></td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule"> Epistaxis</td><td styleCode="Rrule">3 (1%)</td><td styleCode="Rrule">2 (1%)</td><td styleCode="Rrule">0</td></tr><tr styleCode="Botrule"><td colspan="4" styleCode="Lrule Rrule"><content styleCode="bold">Psychiatric Disorders</content></td></tr><tr><td styleCode="Lrule Rrule"> Anxiety</td><td styleCode="Rrule">0</td><td styleCode="Rrule">2 (1%)</td><td styleCode="Rrule">0</td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

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