repotrectinib
Used for Cancer
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Manufactured by various FDA-approved generic manufacturers.
*You can pay as little as $0 per fill using Drug Coupons or Patient Assistance Programs. Subject to applicability & eligibility requirements.
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repotrectinib Uses, Side Effects, Interactions, Warnings & Dosing
What dosages is repotrectinib available in?
repotrectinib is available as a 40 mg oral capsule.
What is repotrectinib used for?
repotrectinib is a kinase inhibitor indicated for the treatment of adult patients with locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC).
How does repotrectinib work?
repotrectinib works by blocking a protein that causes cancer cells to grow and multiply. This helps to slow or stop the spread of cancer cells.
How do I take repotrectinib?
repotrectinib is typically dosed as 160 mg orally once daily for 14 days, then increase to 160 mg twice daily, with or without food.
Is it safe for me to take repotrectinib?
repotrectinib is a safe and effective treatment when used for FDA licensed indications. However, like all medications, they may give you unwanted side effects. You should always discuss potential side effects with your physician to ensure the medication is suitable and right for you.
repotrectinib Common Side Effects
Common side effects of repotrectinib:
- Dizziness
- Foul or metallic taste in your mouth
- Peripheral neuropathy
- Constipation
- Shortness of breath
- Loss of coordination
- Fatigue
- Confusion
- Muscular weakness
repotrectinib Serious Side Effects
Serious side effects are rare with repotrectinib. Contact your doctor right away if you experience any of the following.
- Central nervous system (CNS) effects
- Lung problems
- Liver problems
- Muscles problems
- Increase uric acid
- Bone fractures
Effects of other drugs, drug classes and over-the-counter products on repotrectinib
The following medications may interact with repotrectinib:
- Strong and Moderate CYP3A Inhibitors: Avoid concomitant use
- P-gp inhibitors: Avoid concomitant use.
- Strong and Moderate CYP3A Inducers: Avoid concomitant use
- Certain CYP3A Substrates: Avoid concomitant use with CYP3A substrates, where minimal concentration changes can cause reduced efficacy
- Hormonal contraceptives: Avoid concomitant use
Who makes repotrectinib?
Various FDA-approved generic manufacturers
Is repotrectinib safe in pregnancy?
repotrectinib can harm your unborn baby. Tell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with repotrectinib.
Females who are able to become pregnant: Your healthcare provider should do a pregnancy test before you start treatment with repotrectinib. You should use effective non-hormonal birth control (contraception) during treatment and for 2 months after the last dose of repotrectinib.
Birth control methods that contain hormones (such as birth control pills, injections or transdermal system patches)
may not work as well during treatment with repotrectinib.
Talk to your healthcare provider about birth control methods that may be right for you. Males with female partners who are able to become pregnant: You should use effective birth control during treatment with repotrectinib and for 4 months after the last dose.
What is the brand name for repotrectinib?
The FDA's medical product safety reporting program for health professionals, patients and consumers.
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Medical Disclaimer
NowPatient has taken all reasonable steps to ensure that all material is factually accurate, complete, and current. However, the knowledge and experience of a qualified healthcare professional should always be sought after instead of using the information on this page. Before taking any drug, you should always speak to your doctor or another qualified healthcare provider.
The information provided here about medications is subject to change and is not meant to include all uses, precautions, warnings, directions, drug interactions, allergic reactions, or negative effects. The absence of warnings or other information for a particular medication does not imply that the medication or medication combination is appropriate for all patients or for all possible purposes.
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