Provided by You Health
Topical Finasteride 0.3% + Minoxidil 6% Spray
Following consultation, a You Health provider determined that Topical Finasteride + Minoxidil Spray is medically appropriate and necessary for your treatment.
This medication overview contains information regarding the medication that was prescribed to you including but not limited to: ingredient information, interactions, side effects, instructions for use, and other important information you should know prior to starting it.
The female-pattern hair loss (androgenic alopecia) treatment that you have been prescribed is designed to help prevent hair loss and promote new hair growth in cisgender women, trans men, and trans women. It is a topical treatment alternative to oral finasteride that emerging research studies have shown is a safe and effective option to treat female-pattern hair loss.
Unlike oral finasteride (which is FDA-approved only for use in men), topical finasteride + minoxidil spray is a compounded product and has not been approved by the FDA. It is only available if a healthcare provider has determined that this treatment is medically appropriate for you after an online consultation with a medical provider through the Hers platform.
Do not use other finasteride or topical minoxidil products while you are using the Topical finasteride 0.3% + minoxidil 6% spray.
Age: 18+
No. Using more than the recommended amount will not improve results and can increase the risk of side effects.
You may experience side effects with this medication. These side effects are typically mild and go away with time and regular use:
These are not all of the possible side effects of topical finasteride + minoxidil spray. For more information, ask your healthcare provider or pharmacist.
Contact your healthcare provider for medical advice about side effects. You can message a healthcare provider through your Hers account if you have any questions about your treatment, including any side effects you may be experiencing. You may report side effects to FDA by calling at 1-800-FDA-1088 or visiting
http://www.fda.gov/MedWatch.
Your provider has evaluated the specific health information you provided and is making recommendations based on it. If you forgot to provide or incorrectly provided any information, your provider may misdiagnose or fail to diagnose conditions that you may have which could affect their recommendation for treatment. If you need to clarify or update any information about your health, please message a provider through the Hers platform.
This treatment is not 100% effective. It may not work or may only partially resolve the condition for which you are seeking treatment. If you do not see any signs of improvement or if you are experiencing new or worsening symptoms, message a provider through the Hers platform anytime or contact your regular healthcare provider. If it is an emergency, call 911 or seek immediate help in-person.
There is also a risk that your provider will misdiagnose or fail to diagnose conditions that you may have which could affect the recommendation for treatment. The healthcare providers providing treatment through the Hers platform use evidence-based guidelines as well as clinical decision-making to try to minimize these risks.
Your provider is recommending this treatment for you because the potential benefits outweigh the risks in their estimation. You should evaluate this information and any input from your in-person healthcare team, and any other relevant information to decide if this treatment plan is appropriate for you. You are free to not follow the recommendations you received from the provider through the Hers platform.
You can request access to your records anytime. We strongly recommend that you update your in-person healthcare team about any new medicines that you are taking or other changes in your health.
You can also ask questions anytime by messaging a provider through the Hers platform, and we are happy to help you share any information about your health with your in-person healthcare team.