ZAVZPRET™ Medication Guide

([zavegepant] nasal spray)

17 PATIENT COUNSELING INFORMATION

Advise patients to read the FDA-approved patient labeling (Patient Information and Instructions for Use).

Hypersensitivity Reactions

Inform patients about the signs and symptoms of hypersensitivity reactions after administration of ZAVZPRET. Advise patients to contact their healthcare provider immediately if signs or symptoms of hypersensitivity reactions occur [see Warnings and Precautions (5.1)].

Drug Interactions

Advise patients to speak with their healthcare provider about any prescription or over-the-counter medications or herbal supplements that they take or plan to take. Inform patients that if they need to use an intranasal decongestant it should be administered at least 1 hour after ZAVZPRET administration [see Drug Interactions (7.3)].

This product’s labeling may have been updated. For the most recent prescribing information, please visit www.pfizer.com.

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LAB-1544-1.0

Patient Package Insert

This Patient Information has been approved by the US. Food and Drug Administration

3/2023

PATIENT INFORMATION
ZAVZPRET™ (zav-spret)

(zavegepant)

nasal spray

What is ZAVZPRET?

ZAVZPRET is a prescription medicine used in adults for the acute treatment of migraine attacks with or without aura.

ZAVZPRET is not used to prevent migraine attacks.

It is not known if ZAVZPRET is safe and effective in children.

Do not use ZAVZPRET if you are:

allergic to zavegepant, or any of the ingredients in ZAVZPRET.

See the end of this leaflet for a complete list of ingredients in ZAVZPRET.

Before you use ZAVZPRET, tell your healthcare provider about all of your medical conditions, including if you:

have kidney problems.
have liver problems.
are pregnant or plan to become pregnant. It is not known if ZAVZPRET will harm your unborn baby.
are breastfeeding or plan to breastfeed. It is not known whether ZAVZPRET passes into your breast milk. Talk with your healthcare provider about the best way to feed your baby if you use ZAVZPRET.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

How should I use ZAVZPRET?

Use ZAVZPRET exactly how your healthcare provider tells you to use it.
See the Instructions for Use for complete information on how to use ZAVZPRET nasal spray.
ZAVZPRET is given in the nose (nasal) only.
Each ZAVZPRET only sprays 1 time and cannot be reused. Do not test or prime the nasal spray before use.
Each dose of ZAVZPRET is provided in an individual pack. Use all of the medicine in 1 pack for a complete dose.
The recommended dose is 10 mg given as a single spray in one nostril.
Do not use more than 1 spray (10 mg) of ZAVZPRET nasal spray in a 24-hour period.
It is not known if it is safe to use more than 8 sprays (doses) of ZAVZPRET in 30 days.
Avoid using intranasal decongestants with ZAVZPRET. If you have to use an intranasal decongestant, use it at least 1 hour after using ZAVZPRET.

What are the possible side effects of ZAVZPRET?

ZAVZPRET may cause serious side effects including:

Allergic reactions. Allergic reactions, including hives and swelling of the face, can happen after you use ZAVZPRET. Call your healthcare provider or get emergency help right away if you have any of the following symptoms, which may be part of an allergic reaction:
o
swelling of the face, mouth, tongue, or throat
o
trouble breathing

The most common side effects of ZAVZPRET are:

unusual taste
nausea
nasal discomfort
vomiting

These are not the only possible side effects of ZAVZPRET.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1 800-FDA-1088.

How should I store ZAVZPRET?

Store ZAVZPRET in the blister package that it comes in.
Store ZAVZPRET at room temperature between 68°F to 77°F (20°C to 25°C).
Do not freeze.

Keep ZAVZPRET and all medicines out of the reach of children.

General information about the safe and effective use of ZAVZPRET:

Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use ZAVZPRET for a condition for which it was not prescribed. Do not give ZAVZPRET to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about ZAVZPRET that is written for health professionals.

What are the ingredients in ZAVZPRET?

Active ingredients in ZAVZPRET: zavegepant

Inactive ingredients in ZAVZPRET: dextrose, hydrochloric acid, sodium hydroxide, and succinic acid in water for injection.

Logo

For more information, go to www.zavzpret.com or call 1-800-438-1985.

LAB-1545-1.0

Find ZAVZPRET™ medical information:

Find ZAVZPRET™ medical information:

Our scientific content is evidence-based, scientifically balanced and non-promotional. It undergoes rigorous internal medical review and is updated regularly to reflect new information.

ZAVZPRET™ Quick Finder

Prescribing Information
Download Prescribing Information

Health Professional Information

Medication Guide

17 PATIENT COUNSELING INFORMATION

Advise patients to read the FDA-approved patient labeling (Patient Information and Instructions for Use).

Hypersensitivity Reactions

Inform patients about the signs and symptoms of hypersensitivity reactions after administration of ZAVZPRET. Advise patients to contact their healthcare provider immediately if signs or symptoms of hypersensitivity reactions occur [see Warnings and Precautions (5.1)].

Drug Interactions

Advise patients to speak with their healthcare provider about any prescription or over-the-counter medications or herbal supplements that they take or plan to take. Inform patients that if they need to use an intranasal decongestant it should be administered at least 1 hour after ZAVZPRET administration [see Drug Interactions (7.3)].

This product’s labeling may have been updated. For the most recent prescribing information, please visit www.pfizer.com.

Logo

LAB-1544-1.0

Patient Package Insert

This Patient Information has been approved by the US. Food and Drug Administration

3/2023

PATIENT INFORMATION
ZAVZPRET™ (zav-spret)

(zavegepant)

nasal spray

What is ZAVZPRET?

ZAVZPRET is a prescription medicine used in adults for the acute treatment of migraine attacks with or without aura.

ZAVZPRET is not used to prevent migraine attacks.

It is not known if ZAVZPRET is safe and effective in children.

Do not use ZAVZPRET if you are:

allergic to zavegepant, or any of the ingredients in ZAVZPRET.

See the end of this leaflet for a complete list of ingredients in ZAVZPRET.

Before you use ZAVZPRET, tell your healthcare provider about all of your medical conditions, including if you:

have kidney problems.
have liver problems.
are pregnant or plan to become pregnant. It is not known if ZAVZPRET will harm your unborn baby.
are breastfeeding or plan to breastfeed. It is not known whether ZAVZPRET passes into your breast milk. Talk with your healthcare provider about the best way to feed your baby if you use ZAVZPRET.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

How should I use ZAVZPRET?

Use ZAVZPRET exactly how your healthcare provider tells you to use it.
See the Instructions for Use for complete information on how to use ZAVZPRET nasal spray.
ZAVZPRET is given in the nose (nasal) only.
Each ZAVZPRET only sprays 1 time and cannot be reused. Do not test or prime the nasal spray before use.
Each dose of ZAVZPRET is provided in an individual pack. Use all of the medicine in 1 pack for a complete dose.
The recommended dose is 10 mg given as a single spray in one nostril.
Do not use more than 1 spray (10 mg) of ZAVZPRET nasal spray in a 24-hour period.
It is not known if it is safe to use more than 8 sprays (doses) of ZAVZPRET in 30 days.
Avoid using intranasal decongestants with ZAVZPRET. If you have to use an intranasal decongestant, use it at least 1 hour after using ZAVZPRET.

What are the possible side effects of ZAVZPRET?

ZAVZPRET may cause serious side effects including:

Allergic reactions. Allergic reactions, including hives and swelling of the face, can happen after you use ZAVZPRET. Call your healthcare provider or get emergency help right away if you have any of the following symptoms, which may be part of an allergic reaction:
o
swelling of the face, mouth, tongue, or throat
o
trouble breathing

The most common side effects of ZAVZPRET are:

unusual taste
nausea
nasal discomfort
vomiting

These are not the only possible side effects of ZAVZPRET.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1 800-FDA-1088.

How should I store ZAVZPRET?

Store ZAVZPRET in the blister package that it comes in.
Store ZAVZPRET at room temperature between 68°F to 77°F (20°C to 25°C).
Do not freeze.

Keep ZAVZPRET and all medicines out of the reach of children.

General information about the safe and effective use of ZAVZPRET:

Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use ZAVZPRET for a condition for which it was not prescribed. Do not give ZAVZPRET to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about ZAVZPRET that is written for health professionals.

What are the ingredients in ZAVZPRET?

Active ingredients in ZAVZPRET: zavegepant

Inactive ingredients in ZAVZPRET: dextrose, hydrochloric acid, sodium hydroxide, and succinic acid in water for injection.

Logo

For more information, go to www.zavzpret.com or call 1-800-438-1985.

LAB-1545-1.0

Medication Guide
Download Consumer Medicine Information

Health Professional Information

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Report Adverse Event

Pfizer Safety

To report an adverse event related to the Pfizer-BioNTech COVID-19 Vaccine, and you are not part of a clinical trial* for this product, click the link below to submit your information:

Pfizer Safety Reporting Site

*If you are involved in a clinical trial for this product, adverse events should be reported to your coordinating study site.

If you cannot use the above website, or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at (800) 438-1985.

FDA Medwatch

You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatch or call (800) 822-7967.