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55130 Van Dyke Ave. #25
Shelby Township,
MI 48016
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55390 Van Dyke Ave. #25
Shelby Township,
MI 48016
Most side effects of LIPO-B are generally mild in nature and dissipate within a short time frame following administration.
Most common LIPO-B side effects
If irritation continues to occur, apply an over-the-counter itch cream, preferably with hydrocortisone, or discontinue use entirely.
In more rare yet severe cases, you may experience irregular heartbeat or trouble breathing. If this happens, discontinue use immediately and contact your healthcare provider.
Other important safety information
Do not use LIPO-B if you are currently pregnant, breastfeeding or plan to become pregnant or breastfeed.
Note: The above statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
According to the National Institutes of Health, carnitine interacts with pivalate-conjugated antibiotics such as pivampicillin which are used in the treatment of urinary tract infections. Taking these antibiotics increases the excretion of pivaloyl-carnitine, which can lead to carnitine depletion. Carnitine also interacts with the anticonvulsants valproic acid, phenobarbital, phenytoin, or carbamazepine. Taking these have been shown to significantly decrease blood levels of carnitine. In addition, the use of valproic acid with or without other anticonvulsants may cause hepatotoxicity and increase plasma ammonia concentrations, leading to encephalopathy.
Some serious side effects may include:
Compounded drugs are permitted to be prescribed under federal law but are not FDA-approved and do not undergo safety, effectiveness, or manufacturing review. Your Custom Health Centers-affiliated provider may recommend certain doses of compounded Tirzepatide based on your medical evaluation.
In rats, Tirzepatide (known as Zepbound®) caused thyroid tumors, including thyroid cancer. It is not known if Tirzepatide will cause thyroid tumors or medullary thyroid carcinoma (MTC) in people. Inform your provider if you notice a lump or swelling in your neck, hoarseness, trouble swallowing, or shortness of breath, as these may be symptoms of thyroid cancer.
Do not use Tirzepatide if you or any family member have had MTC or if you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
Tirzepatide is used along with a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial body mass index (BMI) of:
Limitations of Use:
Do not use Tirzepatide if:
Tirzepatide can be taken with or without food. The pre-filled injector pen is self-administered as a subcutaneous injection in the stomach, thigh, or upper arm once a week on the same day every week. Your Custom Health Centers-affiliated provider will guide you on a treatment regimen that may include dose adjustments every four weeks.
Do not alter your dosing regimen or stop taking Tirzepatide without consulting your provider.
It’s important to inform your Custom Health Centers-affiliated provider of all medications you are taking, including prescription, over-the-counter, vitamins, and herbal supplements.
Be mindful of the following:
Share your complete medical history, especially if you have:
Notify your provider if you are pregnant, planning to become pregnant, or breastfeeding:
Pregnancy registry: A pregnancy exposure registry monitors outcomes in women exposed to Tirzepatide during pregnancy. Pregnant patients and healthcare providers can contact Eli Lilly and Company at 1-800-LillyRx (1-800-545-5979).
Providing inaccurate health information to obtain treatment may result in harm, including death.
If you experience a medical emergency, call 911 or seek immediate medical attention.
These serious side effects are rare but can occur with Tirzepatide. Monitor for these, especially at the start of treatment or with dose changes:
Report negative side effects to the FDA: Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
This information is not comprehensive. Please see the full Prescribing Information for complete safety details.
Compounded drugs are permitted to be prescribed under federal law but are not FDA-approved and do not undergo safety, effectiveness, or manufacturing review. Your Custom Health Centers-affiliated provider may recommend certain doses of compounded Semaglutide based on your medical evaluation.
In studies with mice and rats, Semaglutide (the active ingredient in Wegovy and Ozempic) caused thyroid tumors, including thyroid cancer. It is unknown if Semaglutide will cause thyroid tumors or medullary thyroid carcinoma (MTC) in people. Inform your provider if you notice a lump or swelling in your neck, hoarseness, trouble swallowing, or shortness of breath, as these may be symptoms of thyroid cancer.
Do not use Semaglutide if you or any family member have had MTC or if you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
Semaglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist used for chronic weight management, alongside a reduced-calorie diet and increased physical activity, for people with an initial body mass index (BMI) of:
Limitations of Use:
Do not use Semaglutide if:
Semaglutide can be taken with or without food. It is self-administered as a subcutaneous injection in the stomach, thigh, or upper arm once a week on the same day every week. For detailed instructions, refer to your treatment plan or contact your Custom Health Centers-affiliated provider. They will guide you on your treatment regimen, which may include dose adjustments every four weeks.
Do not alter your dosing regimen or stop taking Semaglutide without consulting your provider.
It’s important to inform your Custom Health Centers-affiliated provider of all medications you are taking, including prescription, over-the-counter, vitamins, and herbal supplements.
Be mindful of the following:
Share your complete medical history, especially if you have:
Notify your provider if you are pregnant, planning to become pregnant, or breastfeeding:
Providing inaccurate health information to obtain treatment may result in harm, including death.
If you experience a medical emergency, call 911 or seek immediate medical attention.
Monitor for these serious side effects, especially at the start of treatment or with dose changes:
Never share needles or syringes to avoid infection risk.
Report negative side effects to the FDA: Call 1-800-FDA-1088 or visit www.fda.gov/medwatch.
This information is not comprehensive. Please see the full Consumer Medical Information for complete safety details.
All medications have the potential for side effects. Side effects may vary based on the individual.
Most common GSH side effects
If irritation at the injection site occurs, you can: consider alternating injection sites on the body, apply an over-the-counter itch cream (preferably with hydrocortisone), use injections less frequently, or discontinue use entirely.
Signs of an allergic reaction to glutathione may include hives, itching, swelling of the face or lips, tongue or throat, or difficulty breathing. If any of this occurs, discontinue use and seek emergency care.
Other important safety information
Taking glutathione long-term may lead to lower zinc levels. Avoid taking glutathione if you’re sensitive to it or allergic to any related ingredients. Do not use GSH if you are pregnant or breastfeeding.
Note: The above statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
The most common side effect of B12 injections is irritation at the injection site. If this occurs, consider changing placement on the body or use injections less often.
For a complete list of possible side effects, click here.
Do not use B12 injections if you are currently pregnant, breastfeeding or plan to become pregnant or breastfeed.
Note: The above statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
A literature review shows there may be evidence of increased depressive symptoms in individuals younger than age 45 while using finasteride for hair loss. Patients with new or worsening depression should stop finasteride use and follow up with their health care provider or a mental health therapist. Source: MedPageToday.org
Depression: A literature review shows there may be evidence of increased depressive symptoms in users younger than age 45 while using finasteride for hair loss. Patients with new or worsening depression should stop finasteride use and follow up with their health care provider or a mental health therapist. Source: MedPageToday.org
While NAD+ supplements have shown promise in supporting cellular health and combating the effects of aging, it is essential to be aware of some important safety information before starting supplementation:
Sildenafil is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED).
Do not use sildenafil if:
Sildenafil can be taken with or without food. Take about 30 minutes to 1 hour before anticipated sexual activity.
Sildenafil has certain drug interactions. It’s important to tell your Custom Health Centers-affiliated provider all of the medications you are currently taking, including prescription, over-the-counter medications, vitamins, and herbal and dietary supplements.
Some medications to watch out for include:
It’s important to share your entire medical history with your provider. In particular, tell your provider if you have or have a past history of:
Withholding or providing inaccurate information about your health and medical history in order to obtain treatment may result in harm, including, in some cases, death.
If you are experiencing a medical emergency, call 911 or seek immediate medical attention.
You or a caregiver should carefully monitor for these side effects, especially at the beginning of treatment:
You are encouraged to report negative side effects of prescription products to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
This information is not comprehensive. Please see the full Prescribing Information for complete safety information.
Tadalafil is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED).
Do not use tadalafil if:
Tadalafil can be taken with or without food. Limit the amount of alcohol to less than 5 drinks.
Do not take tadalafil more than once in a 24-hour period or within 24 hours of any other ED medications or PDE-5 inhibitors. Take the medication exactly as prescribed. If your symptoms are not improving or you have any questions about changing or stopping medication, reach out to your Custom Health Centers-affiliated provider for guidance.
Tadalafil has certain drug interactions. It’s important to tell your Custom Health Centers-affiliated provider about all the medications you are currently taking, including prescription, over-the-counter medications, vitamins, and herbal and dietary supplements.
Some medications to watch out for include:
It’s important to share your entire medical history with your provider. In particular, tell your provider if you have or have a past history of:
Withholding or providing inaccurate information about your health and medical history to obtain treatment may result in harm, including, in some cases, death.
If you are experiencing a medical emergency, call 911 or seek immediate medical attention.
You or a caregiver should carefully monitor for these side effects, especially at the beginning of treatment:
You are encouraged to report negative side effects of prescription products to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
This information is not comprehensive. Please see the full Prescribing Information for complete safety information.
