Hair Regrowth Treatment for Women Side Effects
Generic name: minoxidil topical
Note: This document contains side effect information about minoxidil topical. Some of the dosage forms listed on this page may not apply to the brand name Hair Regrowth Treatment for Women.
Some side effects of Hair Regrowth Treatment for Women may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA.
For the Consumer
Applies to minoxidil topical: topical foam, topical solution
If you experience any of the following serious side effects, stop using minoxidil topical (the active ingredient contained in Hair Regrowth Treatment for Women) and seek emergency medical attention:
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an allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives);
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chest pain;
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irregular or very fast heartbeats;
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dizziness or lightheadedness; or
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fainting.
Continue to use minoxidil topical and talk to your doctor when it is convenient if you experience
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itching, redness, dryness, or flaking of the scalp; or
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a headache.
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.
For Healthcare Professionals
Applies to minoxidil topical: topical foam, topical solution
General
Minoxidil topical (the active ingredient contained in Hair Regrowth Treatment for Women) is generally well tolerated. Dermatological adverse events are the only side effects reported more commonly as compared to placebo.
Cardiovascular
Edema, salt and water retention, pericardial effusion, pericarditis, tamponade, tachycardia, and angina have been reported with oral minoxidil. Patients with underlying heart disease may be at increased risk for these or other cardiovascular adverse effects.
Rarely, cardiovascular side effects have included edema, chest pain, blood pressure changes, palpitations, and changes in pulse rate with minoxidil topical therapy.
Local
Despite low levels of systemic absorption, in one study of 35 men using either topical minoxidil 2% twice a day or placebo for 6 months, minoxidil was associated with cardiac changes, such as significant increases in left ventricular end-diastolic volume, cardiac output, and left ventricular mass.
Systemic side effects are uncommon since very little minoxidil is absorbed after topical application. In one study, the serum levels after 2.5 mg twice a day oral versus 2% twice a day topical minoxidil were 32.8 and 1.7 ng per mL, respectively.
Exacerbation of hair loss/alopecia has been reported.
Dermatologic
Rare cases of generalized hypertrichosis have been associated with topically applied minoxidil. Eczema, irritant dermatitis, and allergic contact dermatitis have also been reported.
Hypersensitivity
Nonspecific allergic reactions, hives, allergic rhinitis, facial swelling, and sensitivity to minoxidil topical (the active ingredient contained in Hair Regrowth Treatment for Women) have rarely been reported.
Nervous system
Headache, dizziness, faintness, and light-headedness have been reported with minoxidil topical (the active ingredient contained in Hair Regrowth Treatment for Women)
Gastrointestinal
Diarrhea, nausea, and vomiting have been reported during treatment with minoxidil topical (the active ingredient contained in Hair Regrowth Treatment for Women)
Ocular
Visual disturbances, including decreased visual acuity, have been reported.
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