TIVDAK® Full Patient Information

(tisotumab vedotin-tftv)

Full Patient Information

17 PATIENT COUNSELING INFORMATION

Advise the patient to read the FDA-approved patient labeling (Medication Guide).

Ocular Adverse Reactions

Inform patients about the eye exam they will receive with an eye care provider before starting TIVDAK, before each of the first nine cycles and as clinically indicated [see Warnings and Precautions (5.1)].
Inform patients about the ocular signs or symptoms the eye care provider will review before each cycle [see Warnings and Precautions (5.1)].
Inform patients that ocular adverse reactions may occur during treatment with TIVDAK and to contact their healthcare provider if they experience new or worsening ocular signs and symptoms [see Warnings and Precautions (5.1)].
Instruct patients to bring their eye drops to each infusion and advise on how to administer the eye drops throughout treatment [see Dosage and Administration (2.2) and Warnings and Precautions (5.1)].
Inform patients to avoid wearing contact lenses during treatment unless directed by an eye care provider [see Dosage and Administration (2.2)].

Peripheral Neuropathy

Advise patients to report to their healthcare provider any numbness and tingling of the hands or feet or muscle weakness [see Warnings and Precautions (5.2)].

Hemorrhage

Instruct patients to contact their healthcare provider to seek immediate medical attention for signs or symptoms of unusual severe bleeding or hemorrhage [see Warnings and Precautions (5.3)].

Pneumonitis

Advise patients to immediately report new or worsening respiratory symptoms [see Warnings and Precautions (5.4)].

Severe Cutaneous Adverse Reactions

Inform patients of the signs and symptoms of severe cutaneous adverse reactions, including life-threatening and potentially fatal SJS, which include target lesions, worsening skin reactions, blistering or peeling of the skin, painful sores in mouth, nose, throat, or genital area, fever or flu-like symptoms, and swollen lymph nodes [see Warnings and Precautions (5.5)].
Instruct patients to contact their healthcare provider to seek immediate medical attention for signs or symptoms of severe cutaneous adverse reactions, including SJS [see Warnings and Precautions (5.5)].

Embryo-Fetal Toxicity

Advise pregnant women and females of reproductive potential of the potential risk to the fetus. Advise patients to inform their healthcare providers of a known or suspected pregnancy [see Warnings and Precautions (5.6) and Use in Specific Populations (8.1)].
Advise females of reproductive potential to use effective contraception during treatment and for 2 months after the last dose. Advise male patients with female partners of reproductive potential to use effective contraception during treatment and for 4 months after the last dose [see Use in Specific Populations (8.1, 8.3)].

Lactation

Advise women not to breastfeed during treatment with TIVDAK and for 3 weeks after the last dose [see Use in Specific Populations (8.2)].

Manufactured by:
Seagen Inc.
Bothell, WA 98021
1-855-4SEAGEN

Marketed by:
Seagen Inc.
Bothell, WA 98021
and
Genmab US, Inc.
Plainsboro, NJ 08536

U.S. License 2257
TIVDAK® is a trademark owned by Seagen Inc.
©2024 Seagen Inc. and Genmab US, Inc.
USPI-761208-v04

SPL MEDGUIDE SECTION

This Medication Guide has been approved by the U.S. Food and Drug Administration.		Revised: 04/2024
MEDICATION GUIDE TIVDAK (TIV-dack) (tisotumab vedotin-tftv) for injection, for intravenous use
What is the most important information I should know about TIVDAK? TIVDAK can cause serious side effects, including: Eye problems. Eye problems are common with TIVDAK, and can also be severe. TIVDAK can cause changes to the surface of your eye that can lead to dry eyes, eye redness, eye irritation, corneal ulcers, blurred vision, and severe vision loss. Tell your healthcare provider if you develop new or worsening vision changes or eye problems during treatment with TIVDAK. Your healthcare provider will send you to an eye specialist to check your eyes before you start treatment with TIVDAK, before each infusion for your first 9 infusions of TIVDAK, and as needed for any new or worsening signs or symptoms of eye problems. Your healthcare provider will ask if you have any signs or symptoms of eye problems before each infusion. You will be referred to an eye specialist for any new or worsening signs or symptoms of eye problems. Your healthcare provider will prescribe 3 different types of eye drops before you start treatment with TIVDAK. Bring the eye drops with you to each infusion and use them as directed by your healthcare provider to reduce your risk of eye problems: Use 1 drop of steroid eye drops in each eye before each infusion and continue to use your eye drops 3 times a day for 3 days after each infusion. Use vasoconstrictor eye drops right before each infusion. Use lubricating eye drops throughout treatment and for 30 days after your last dose of TIVDAK. Do not wear contact lenses throughout your treatment with TIVDAK unless you are told to use them by your eye specialist. See "What are the possible side effects of TIVDAK?" for more information about side effects.
What is TIVDAK? TIVDAK is a prescription medicine used to treat adults with cervical cancer: that has returned or has spread to other parts of the body, and who have received chemotherapy that did not work or is no longer working. It is not known if TIVDAK is safe and effective in children.
Before receiving TIVDAK, tell your healthcare provider about all of your medical conditions, including if you:
have a history of vision or eye problems have numbness or tingling in your hands or feet have bleeding problems have liver problems are pregnant or plan to become pregnant. TIVDAK can harm your unborn baby. Tell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with TIVDAK. Females who are able to become pregnant: Your healthcare provider should do a pregnancy test before you start treatment with TIVDAK. You should use an effective birth control during treatment and for 2 months after your last dose of TIVDAK. Males with female partners who are able to become pregnant: You should use an effective birth control during treatment and for 4 months after your last dose of TIVDAK. are breastfeeding or plan to breastfeed. It is not known if TIVDAK passes into your breast milk. Do not breastfeed during treatment and for 3 weeks after your last dose of TIVDAK. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking TIVDAK with certain other medicines may cause side effects.
How will I receive TIVDAK?
TIVDAK will be given to you by intravenous (IV) infusion into your vein over 30 minutes. TIVDAK is usually given every 3 weeks. Your healthcare provider will decide how many infusions you need. Your healthcare provider will put cold packs on your eyes during each infusion. Your healthcare provider may decrease your dose, temporarily stop, or completely stop treatment with TIVDAK if you have side effects.
What are the possible side effects of TIVDAK? TIVDAK can cause serious side effects, including:
See “What is the most important information I should know about TIVDAK?” Peripheral neuropathy. Nerve problems called peripheral neuropathy are common with TIVDAK, and can also be serious. Tell your healthcare provider right away if you get numbness or tingling in your hands or feet or muscle weakness. Bleeding (hemorrhage). Bleeding problems are common with TIVDAK, and can also be serious. Tell your healthcare provider or get medical help right away if you get signs or symptoms of bleeding during treatment with TIVDAK, including:
blood in your stools or black stools (looks like tar) blood in your urine cough up or vomit blood	unusual vaginal bleeding any unusual or heavy bleeding
Lung problems. TIVDAK may cause severe or life-threatening inflammation of the lungs that can lead to death. Tell your healthcare provider right away if you get new or worsening symptoms, including trouble breathing, shortness of breath, or cough. Severe skin reactions. TIVDAK may cause severe or life-threatening skin reactions that can lead to death. Tell your healthcare provider or get medical help right away if you get signs or symptoms of a severe skin reaction during treatment with TIVDAK, including:
skin reactions that look like rings (target lesions) rash or itching that continues to get worse blistering or peeling of the skin painful sores or ulcers in your mouth, nose, throat, or genital area	fever or flu-like symptoms swollen lymph nodes
The most common side effects of TIVDAK include:
decreased red blood cell counts numbness or tingling in your hands or feet eye problems (conjunctival disorders)	nausea tiredness changes in liver function blood tests	nosebleed hair loss (alopecia) bleeding (hemorrhage)
TIVDAK may cause fertility problems in females and males, which may affect your ability to have children. Talk to your healthcare provider if this is a concern for you. These are not all of the possible side effects of TIVDAK. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
General information about the safe and effective use of TIVDAK. Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. If you would like more information about TIVDAK, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about TIVDAK that is written for healthcare professionals.
What are the ingredients in TIVDAK? Active ingredient: tisotumab vedotin-tftv Inactive ingredients: d-mannitol, l-histidine, l-histidine monohydrochloride, and sucrose. Manufactured by: Seagen Inc., Bothell, WA 98021 Marketed by: Seagen Inc., Bothell, WA 98021 and Genmab US, Inc., Plainsboro, NJ 08536 U.S. License 2257 TIVDAK is a trademark owned by Seagen Inc. ©2024 Seagen Inc. and Genmab US, Inc. MG-761208-v04 For more information, go to www.tivdak.com or call 1-855-4SEAGEN

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Medication Guide

Health Professional Information

Full Patient Information

17 PATIENT COUNSELING INFORMATION

Advise the patient to read the FDA-approved patient labeling (Medication Guide).

Ocular Adverse Reactions

Inform patients about the eye exam they will receive with an eye care provider before starting TIVDAK, before each of the first nine cycles and as clinically indicated [see Warnings and Precautions (5.1)].
Inform patients about the ocular signs or symptoms the eye care provider will review before each cycle [see Warnings and Precautions (5.1)].
Inform patients that ocular adverse reactions may occur during treatment with TIVDAK and to contact their healthcare provider if they experience new or worsening ocular signs and symptoms [see Warnings and Precautions (5.1)].
Instruct patients to bring their eye drops to each infusion and advise on how to administer the eye drops throughout treatment [see Dosage and Administration (2.2) and Warnings and Precautions (5.1)].
Inform patients to avoid wearing contact lenses during treatment unless directed by an eye care provider [see Dosage and Administration (2.2)].

Peripheral Neuropathy

Advise patients to report to their healthcare provider any numbness and tingling of the hands or feet or muscle weakness [see Warnings and Precautions (5.2)].

Hemorrhage

Instruct patients to contact their healthcare provider to seek immediate medical attention for signs or symptoms of unusual severe bleeding or hemorrhage [see Warnings and Precautions (5.3)].

Pneumonitis

Advise patients to immediately report new or worsening respiratory symptoms [see Warnings and Precautions (5.4)].

Severe Cutaneous Adverse Reactions

Inform patients of the signs and symptoms of severe cutaneous adverse reactions, including life-threatening and potentially fatal SJS, which include target lesions, worsening skin reactions, blistering or peeling of the skin, painful sores in mouth, nose, throat, or genital area, fever or flu-like symptoms, and swollen lymph nodes [see Warnings and Precautions (5.5)].
Instruct patients to contact their healthcare provider to seek immediate medical attention for signs or symptoms of severe cutaneous adverse reactions, including SJS [see Warnings and Precautions (5.5)].

Embryo-Fetal Toxicity

Advise pregnant women and females of reproductive potential of the potential risk to the fetus. Advise patients to inform their healthcare providers of a known or suspected pregnancy [see Warnings and Precautions (5.6) and Use in Specific Populations (8.1)].
Advise females of reproductive potential to use effective contraception during treatment and for 2 months after the last dose. Advise male patients with female partners of reproductive potential to use effective contraception during treatment and for 4 months after the last dose [see Use in Specific Populations (8.1, 8.3)].

Lactation

Advise women not to breastfeed during treatment with TIVDAK and for 3 weeks after the last dose [see Use in Specific Populations (8.2)].

Manufactured by:
Seagen Inc.
Bothell, WA 98021
1-855-4SEAGEN

Marketed by:
Seagen Inc.
Bothell, WA 98021
and
Genmab US, Inc.
Plainsboro, NJ 08536

U.S. License 2257
TIVDAK® is a trademark owned by Seagen Inc.
©2024 Seagen Inc. and Genmab US, Inc.
USPI-761208-v04

SPL MEDGUIDE SECTION

This Medication Guide has been approved by the U.S. Food and Drug Administration.		Revised: 04/2024
MEDICATION GUIDE TIVDAK (TIV-dack) (tisotumab vedotin-tftv) for injection, for intravenous use
What is the most important information I should know about TIVDAK? TIVDAK can cause serious side effects, including: Eye problems. Eye problems are common with TIVDAK, and can also be severe. TIVDAK can cause changes to the surface of your eye that can lead to dry eyes, eye redness, eye irritation, corneal ulcers, blurred vision, and severe vision loss. Tell your healthcare provider if you develop new or worsening vision changes or eye problems during treatment with TIVDAK. Your healthcare provider will send you to an eye specialist to check your eyes before you start treatment with TIVDAK, before each infusion for your first 9 infusions of TIVDAK, and as needed for any new or worsening signs or symptoms of eye problems. Your healthcare provider will ask if you have any signs or symptoms of eye problems before each infusion. You will be referred to an eye specialist for any new or worsening signs or symptoms of eye problems. Your healthcare provider will prescribe 3 different types of eye drops before you start treatment with TIVDAK. Bring the eye drops with you to each infusion and use them as directed by your healthcare provider to reduce your risk of eye problems: Use 1 drop of steroid eye drops in each eye before each infusion and continue to use your eye drops 3 times a day for 3 days after each infusion. Use vasoconstrictor eye drops right before each infusion. Use lubricating eye drops throughout treatment and for 30 days after your last dose of TIVDAK. Do not wear contact lenses throughout your treatment with TIVDAK unless you are told to use them by your eye specialist. See "What are the possible side effects of TIVDAK?" for more information about side effects.
What is TIVDAK? TIVDAK is a prescription medicine used to treat adults with cervical cancer: that has returned or has spread to other parts of the body, and who have received chemotherapy that did not work or is no longer working. It is not known if TIVDAK is safe and effective in children.
Before receiving TIVDAK, tell your healthcare provider about all of your medical conditions, including if you:
have a history of vision or eye problems have numbness or tingling in your hands or feet have bleeding problems have liver problems are pregnant or plan to become pregnant. TIVDAK can harm your unborn baby. Tell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with TIVDAK. Females who are able to become pregnant: Your healthcare provider should do a pregnancy test before you start treatment with TIVDAK. You should use an effective birth control during treatment and for 2 months after your last dose of TIVDAK. Males with female partners who are able to become pregnant: You should use an effective birth control during treatment and for 4 months after your last dose of TIVDAK. are breastfeeding or plan to breastfeed. It is not known if TIVDAK passes into your breast milk. Do not breastfeed during treatment and for 3 weeks after your last dose of TIVDAK. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking TIVDAK with certain other medicines may cause side effects.
How will I receive TIVDAK?
TIVDAK will be given to you by intravenous (IV) infusion into your vein over 30 minutes. TIVDAK is usually given every 3 weeks. Your healthcare provider will decide how many infusions you need. Your healthcare provider will put cold packs on your eyes during each infusion. Your healthcare provider may decrease your dose, temporarily stop, or completely stop treatment with TIVDAK if you have side effects.
What are the possible side effects of TIVDAK? TIVDAK can cause serious side effects, including:
See “What is the most important information I should know about TIVDAK?” Peripheral neuropathy. Nerve problems called peripheral neuropathy are common with TIVDAK, and can also be serious. Tell your healthcare provider right away if you get numbness or tingling in your hands or feet or muscle weakness. Bleeding (hemorrhage). Bleeding problems are common with TIVDAK, and can also be serious. Tell your healthcare provider or get medical help right away if you get signs or symptoms of bleeding during treatment with TIVDAK, including:
blood in your stools or black stools (looks like tar) blood in your urine cough up or vomit blood	unusual vaginal bleeding any unusual or heavy bleeding
Lung problems. TIVDAK may cause severe or life-threatening inflammation of the lungs that can lead to death. Tell your healthcare provider right away if you get new or worsening symptoms, including trouble breathing, shortness of breath, or cough. Severe skin reactions. TIVDAK may cause severe or life-threatening skin reactions that can lead to death. Tell your healthcare provider or get medical help right away if you get signs or symptoms of a severe skin reaction during treatment with TIVDAK, including:
skin reactions that look like rings (target lesions) rash or itching that continues to get worse blistering or peeling of the skin painful sores or ulcers in your mouth, nose, throat, or genital area	fever or flu-like symptoms swollen lymph nodes
The most common side effects of TIVDAK include:
decreased red blood cell counts numbness or tingling in your hands or feet eye problems (conjunctival disorders)	nausea tiredness changes in liver function blood tests	nosebleed hair loss (alopecia) bleeding (hemorrhage)
TIVDAK may cause fertility problems in females and males, which may affect your ability to have children. Talk to your healthcare provider if this is a concern for you. These are not all of the possible side effects of TIVDAK. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
General information about the safe and effective use of TIVDAK. Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. If you would like more information about TIVDAK, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about TIVDAK that is written for healthcare professionals.
What are the ingredients in TIVDAK? Active ingredient: tisotumab vedotin-tftv Inactive ingredients: d-mannitol, l-histidine, l-histidine monohydrochloride, and sucrose. Manufactured by: Seagen Inc., Bothell, WA 98021 Marketed by: Seagen Inc., Bothell, WA 98021 and Genmab US, Inc., Plainsboro, NJ 08536 U.S. License 2257 TIVDAK is a trademark owned by Seagen Inc. ©2024 Seagen Inc. and Genmab US, Inc. MG-761208-v04 For more information, go to www.tivdak.com or call 1-855-4SEAGEN

Prescribing Information

Download Prescribing Information

Health Professional Information

Full Patient Information

17 PATIENT COUNSELING INFORMATION

Advise the patient to read the FDA-approved patient labeling (Medication Guide).

Ocular Adverse Reactions

Inform patients about the eye exam they will receive with an eye care provider before starting TIVDAK, before each of the first nine cycles and as clinically indicated [see Warnings and Precautions (5.1)].
Inform patients about the ocular signs or symptoms the eye care provider will review before each cycle [see Warnings and Precautions (5.1)].
Inform patients that ocular adverse reactions may occur during treatment with TIVDAK and to contact their healthcare provider if they experience new or worsening ocular signs and symptoms [see Warnings and Precautions (5.1)].
Instruct patients to bring their eye drops to each infusion and advise on how to administer the eye drops throughout treatment [see Dosage and Administration (2.2) and Warnings and Precautions (5.1)].
Inform patients to avoid wearing contact lenses during treatment unless directed by an eye care provider [see Dosage and Administration (2.2)].

Peripheral Neuropathy

Advise patients to report to their healthcare provider any numbness and tingling of the hands or feet or muscle weakness [see Warnings and Precautions (5.2)].

Hemorrhage

Instruct patients to contact their healthcare provider to seek immediate medical attention for signs or symptoms of unusual severe bleeding or hemorrhage [see Warnings and Precautions (5.3)].

Pneumonitis

Advise patients to immediately report new or worsening respiratory symptoms [see Warnings and Precautions (5.4)].

Severe Cutaneous Adverse Reactions

Inform patients of the signs and symptoms of severe cutaneous adverse reactions, including life-threatening and potentially fatal SJS, which include target lesions, worsening skin reactions, blistering or peeling of the skin, painful sores in mouth, nose, throat, or genital area, fever or flu-like symptoms, and swollen lymph nodes [see Warnings and Precautions (5.5)].
Instruct patients to contact their healthcare provider to seek immediate medical attention for signs or symptoms of severe cutaneous adverse reactions, including SJS [see Warnings and Precautions (5.5)].

Embryo-Fetal Toxicity

Advise pregnant women and females of reproductive potential of the potential risk to the fetus. Advise patients to inform their healthcare providers of a known or suspected pregnancy [see Warnings and Precautions (5.6) and Use in Specific Populations (8.1)].
Advise females of reproductive potential to use effective contraception during treatment and for 2 months after the last dose. Advise male patients with female partners of reproductive potential to use effective contraception during treatment and for 4 months after the last dose [see Use in Specific Populations (8.1, 8.3)].

Lactation

Advise women not to breastfeed during treatment with TIVDAK and for 3 weeks after the last dose [see Use in Specific Populations (8.2)].

Manufactured by:
Seagen Inc.
Bothell, WA 98021
1-855-4SEAGEN

Marketed by:
Seagen Inc.
Bothell, WA 98021
and
Genmab US, Inc.
Plainsboro, NJ 08536

SPL MEDGUIDE SECTION

This Medication Guide has been approved by the U.S. Food and Drug Administration.		Revised: 04/2024
MEDICATION GUIDE TIVDAK (TIV-dack) (tisotumab vedotin-tftv) for injection, for intravenous use
What is the most important information I should know about TIVDAK? TIVDAK can cause serious side effects, including: Eye problems. Eye problems are common with TIVDAK, and can also be severe. TIVDAK can cause changes to the surface of your eye that can lead to dry eyes, eye redness, eye irritation, corneal ulcers, blurred vision, and severe vision loss. Tell your healthcare provider if you develop new or worsening vision changes or eye problems during treatment with TIVDAK. Your healthcare provider will send you to an eye specialist to check your eyes before you start treatment with TIVDAK, before each infusion for your first 9 infusions of TIVDAK, and as needed for any new or worsening signs or symptoms of eye problems. Your healthcare provider will ask if you have any signs or symptoms of eye problems before each infusion. You will be referred to an eye specialist for any new or worsening signs or symptoms of eye problems. Your healthcare provider will prescribe 3 different types of eye drops before you start treatment with TIVDAK. Bring the eye drops with you to each infusion and use them as directed by your healthcare provider to reduce your risk of eye problems: Use 1 drop of steroid eye drops in each eye before each infusion and continue to use your eye drops 3 times a day for 3 days after each infusion. Use vasoconstrictor eye drops right before each infusion. Use lubricating eye drops throughout treatment and for 30 days after your last dose of TIVDAK. Do not wear contact lenses throughout your treatment with TIVDAK unless you are told to use them by your eye specialist. See "What are the possible side effects of TIVDAK?" for more information about side effects.
What is TIVDAK? TIVDAK is a prescription medicine used to treat adults with cervical cancer: that has returned or has spread to other parts of the body, and who have received chemotherapy that did not work or is no longer working. It is not known if TIVDAK is safe and effective in children.
Before receiving TIVDAK, tell your healthcare provider about all of your medical conditions, including if you:
have a history of vision or eye problems have numbness or tingling in your hands or feet have bleeding problems have liver problems are pregnant or plan to become pregnant. TIVDAK can harm your unborn baby. Tell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with TIVDAK. Females who are able to become pregnant: Your healthcare provider should do a pregnancy test before you start treatment with TIVDAK. You should use an effective birth control during treatment and for 2 months after your last dose of TIVDAK. Males with female partners who are able to become pregnant: You should use an effective birth control during treatment and for 4 months after your last dose of TIVDAK. are breastfeeding or plan to breastfeed. It is not known if TIVDAK passes into your breast milk. Do not breastfeed during treatment and for 3 weeks after your last dose of TIVDAK. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking TIVDAK with certain other medicines may cause side effects.
How will I receive TIVDAK?
TIVDAK will be given to you by intravenous (IV) infusion into your vein over 30 minutes. TIVDAK is usually given every 3 weeks. Your healthcare provider will decide how many infusions you need. Your healthcare provider will put cold packs on your eyes during each infusion. Your healthcare provider may decrease your dose, temporarily stop, or completely stop treatment with TIVDAK if you have side effects.
What are the possible side effects of TIVDAK? TIVDAK can cause serious side effects, including:
See “What is the most important information I should know about TIVDAK?” Peripheral neuropathy. Nerve problems called peripheral neuropathy are common with TIVDAK, and can also be serious. Tell your healthcare provider right away if you get numbness or tingling in your hands or feet or muscle weakness. Bleeding (hemorrhage). Bleeding problems are common with TIVDAK, and can also be serious. Tell your healthcare provider or get medical help right away if you get signs or symptoms of bleeding during treatment with TIVDAK, including:
blood in your stools or black stools (looks like tar) blood in your urine cough up or vomit blood	unusual vaginal bleeding any unusual or heavy bleeding
Lung problems. TIVDAK may cause severe or life-threatening inflammation of the lungs that can lead to death. Tell your healthcare provider right away if you get new or worsening symptoms, including trouble breathing, shortness of breath, or cough. Severe skin reactions. TIVDAK may cause severe or life-threatening skin reactions that can lead to death. Tell your healthcare provider or get medical help right away if you get signs or symptoms of a severe skin reaction during treatment with TIVDAK, including:
skin reactions that look like rings (target lesions) rash or itching that continues to get worse blistering or peeling of the skin painful sores or ulcers in your mouth, nose, throat, or genital area	fever or flu-like symptoms swollen lymph nodes
The most common side effects of TIVDAK include:
decreased red blood cell counts numbness or tingling in your hands or feet eye problems (conjunctival disorders)	nausea tiredness changes in liver function blood tests	nosebleed hair loss (alopecia) bleeding (hemorrhage)
TIVDAK may cause fertility problems in females and males, which may affect your ability to have children. Talk to your healthcare provider if this is a concern for you. These are not all of the possible side effects of TIVDAK. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
General information about the safe and effective use of TIVDAK. Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. If you would like more information about TIVDAK, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about TIVDAK that is written for healthcare professionals.
What are the ingredients in TIVDAK? Active ingredient: tisotumab vedotin-tftv Inactive ingredients: d-mannitol, l-histidine, l-histidine monohydrochloride, and sucrose. Manufactured by: Seagen Inc., Bothell, WA 98021 Marketed by: Seagen Inc., Bothell, WA 98021 and Genmab US, Inc., Plainsboro, NJ 08536 U.S. License 2257 TIVDAK is a trademark owned by Seagen Inc. ©2024 Seagen Inc. and Genmab US, Inc. MG-761208-v04 For more information, go to www.tivdak.com or call 1-855-4SEAGEN

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