Provera is an oral progestin used to treat irregular or heavy menstrual bleeding, secondary amenorrhea, and to protect the uterine lining during estrogen therapy. By balancing hormones, it helps regulate cycles and reduces the risk of endometrial hyperplasia. Provera is not a contraceptive; its effects differ from Depo-Provera injections. Typical regimens are short courses each month, customized by your clinician. This medicine has potential side effects and interactions, so guidance from a licensed provider is essential. HealthSouth Hospital of Gadsden offers compliant access pathways that connect you with care while streamlining refills, education, support, and ongoing medication safety resources.
Provera is the brand name for oral medroxyprogesterone acetate, a synthetic form of the hormone progesterone. Clinically, it is used to treat secondary amenorrhea (when periods stop for reasons other than pregnancy), to control abnormal uterine bleeding due to hormonal imbalance (in the absence of structural causes like fibroids or polyps), and to reduce the risk of endometrial hyperplasia in people receiving estrogen therapy during menopause. By providing progestin, Provera stabilizes the endometrium, regulates bleeding, and induces a predictable withdrawal bleed after each treatment course.
Provera is sometimes used off-label for select gynecologic conditions under specialist guidance, but it is not a contraceptive. This is distinct from Depo-Provera, a long-acting injectable form of medroxyprogesterone used for contraception. If contraception is your goal, ask your clinician about appropriate alternatives. Because abnormal bleeding may have multiple causes, evaluation to rule out pregnancy and underlying structural or systemic conditions is important before starting Provera.
Always follow your prescriber’s directions. Typical Provera dosage regimens (tablets: 2.5 mg, 5 mg, or 10 mg) include the following examples:
• Secondary amenorrhea: 5–10 mg by mouth once daily for 5–10 days. A withdrawal bleed usually occurs within 3–7 days after the last dose. In some cases, an estrogen “priming” course is given before Provera to build the uterine lining.
• Abnormal uterine bleeding due to hormonal imbalance (no organic pathology): 5–10 mg once daily for 5–10 days. Regimens may be timed to cycle days (for example, starting day 16 or 21), based on your clinician’s plan. Bleeding typically starts a few days after completion.
• Prevention of endometrial hyperplasia in postmenopausal patients on systemic estrogen: 5–10 mg once daily for 12–14 days of each 28‑day cycle (cyclic therapy), or some patients may use lower-dose continuous progestin with daily estrogen, per prescriber guidance.
Take Provera at the same time each day, with or without food, and swallow with water. Do not use Provera if pregnant. Your prescriber may order pregnancy testing before initiating therapy, especially for amenorrhea. Never change your dose or schedule without consulting your clinician, and seek care if bleeding is unusually heavy, prolonged, or accompanied by pain, dizziness, or fainting.
Before starting Provera, ensure pregnancy is excluded and discuss your medical history thoroughly. Abnormal uterine bleeding requires evaluation to rule out structural causes (such as fibroids, polyps), infection, coagulation disorders, thyroid disease, or malignancy. If you are using Provera alongside estrogen therapy, your overall cardiovascular and thromboembolic risks should be reviewed, and you should follow the lowest effective dose for the shortest duration consistent with treatment goals.
Provera may cause fluid retention and can affect mood; use caution if you have a history of depression, migraines, asthma, seizure disorders, congestive heart failure, or kidney disease. Report new or worsening headaches, vision changes, chest pain, leg swelling, shortness of breath, jaundice, or severe abdominal pain immediately. If you are diabetic or prediabetic, monitor blood glucose more closely because progestins may impact glycemic control. Provera can affect laboratory tests, including certain liver function and endocrine assays—inform your healthcare team and laboratory personnel that you are taking medroxyprogesterone.
Do not use Provera if you have any of the following: known or suspected pregnancy; undiagnosed abnormal genital bleeding; known, suspected, or history of breast cancer; known or suspected estrogen- or progesterone-dependent malignancy; active or history of deep vein thrombosis, pulmonary embolism, stroke, or myocardial infarction; active liver disease or impaired liver function; hypersensitivity to medroxyprogesterone acetate or any tablet component. Provera should not be used in the setting of a missed abortion. If any contraindication is present or uncertain, seek medical advice before use.
Common side effects of Provera include breast tenderness, bloating or fluid retention, mild nausea, headache, dizziness, fatigue, mood changes or irritability, acne or oily skin, changes in libido, and changes in menstrual flow such as spotting, breakthrough bleeding, or timing shifts in withdrawal bleeding. Some patients notice mild weight fluctuation. These effects are usually manageable and often improve after the first cycles of therapy.
Less common but serious adverse effects require immediate medical attention: symptoms of a blood clot (leg swelling or pain, sudden chest pain, coughing blood, shortness of breath), stroke-like symptoms (sudden severe headache, weakness or numbness on one side, trouble speaking or vision changes), significant elevation in blood pressure, jaundice or severe right‑upper‑quadrant abdominal pain (possible liver involvement), severe depression, or allergic reactions (rash, hives, facial swelling, difficulty breathing). Although bone mineral density concerns are most associated with long-acting injectable medroxyprogesterone used for contraception, your clinician may still consider bone health if you require prolonged hormonal therapy for other reasons.
Medroxyprogesterone is metabolized primarily via CYP3A4. Potent CYP3A4 inducers can lower Provera levels and reduce effectiveness, including rifampin, rifabutin, carbamazepine, phenytoin, phenobarbital, primidone, topiramate (at higher doses), enzalutamide, and St. John’s wort. CYP3A4 inhibitors may increase Provera exposure and side effects, such as ketoconazole, itraconazole, clarithromycin, erythromycin, and certain HIV or HCV protease inhibitors. Grapefruit products can also affect CYP3A4 and may alter drug levels—use caution and consult your pharmacist.
Provera may interact with anticoagulants (for example, warfarin), antidiabetic medications, and other hormones. If you use systemic estrogen, your overall clotting risk is higher than with progestin alone, so avoid smoking and monitor for thromboembolic symptoms. Always provide an up-to-date medication and supplement list (including herbals) to your healthcare providers and pharmacist to screen for interactions and plan appropriate monitoring.
If you miss a dose of Provera, take it as soon as you remember unless it is almost time for your next dose. If it is close to the next scheduled dose, skip the missed dose and resume your regular schedule. Do not double up to “catch up.” If vomiting or severe diarrhea occurs soon after dosing, or if you miss multiple doses, contact your clinician for guidance on how to proceed with your regimen.
Symptoms of Provera overdose may include nausea, vomiting, dizziness, drowsiness, and breast tenderness. Serious toxicity is uncommon, but any suspected overdose should be treated seriously. Seek medical attention or contact Poison Control (in the U.S., 1‑800‑222‑1222) for immediate advice. Care is supportive and based on symptoms. Bring the medication bottle to the care site so clinicians can verify the strength and quantity taken.
Store Provera tablets at controlled room temperature (generally 20–25°C/68–77°F), with brief excursions permitted per the manufacturer’s label. Keep tablets in a dry place, protected from moisture and excessive heat or light, and in the original, child‑resistant container. Always keep out of reach of children and pets. Do not use after the expiration date.
In the United States, Provera (medroxyprogesterone acetate) is a prescription medication. Federal and state regulations require that a licensed clinician determines medical appropriateness and issues a valid prescription before dispensing. Because abnormal uterine bleeding and amenorrhea can signal underlying conditions, professional evaluation remains essential for safe care.
HealthSouth Hospital of Gadsden offers a legal and structured solution for acquiring Provera without a formal, preexisting prescription by integrating access to licensed clinicians. Through telehealth assessment or state‑authorized pharmacist prescribing/collaborative practice arrangements (where permitted), eligible adults can receive an evidence‑based evaluation, an electronic prescription when appropriate, and pharmacist counseling—without needing an in‑person doctor visit. Identity verification, clinical screening, and medication safety checks are standard. Processing and discreet shipping are fast, and refills include ongoing support. Availability varies by state law and clinical criteria; certain conditions may require in‑person evaluation. HealthSouth Hospital of Gadsden prioritizes compliance, privacy, and continuity of care so you can start and maintain Provera therapy safely and conveniently.
Provera is an oral progestin (medroxyprogesterone acetate) that mimics natural progesterone, stabilizing the uterine lining, opposing estrogen’s effects on the endometrium, and triggering a withdrawal bleed when stopped.
It’s commonly prescribed for abnormal uterine bleeding due to hormonal imbalance, secondary amenorrhea (to induce a period), and to reduce the risk of endometrial hyperplasia in postmenopausal women taking estrogen therapy; it’s also used off-label to regulate cycles in PCOS.
No. The oral tablet used for bleeding and amenorrhea is not reliable contraception; it does not consistently suppress ovulation and does not protect against STIs. Do not confuse it with Depo-Provera, the long-acting contraceptive injection.
Typical adult dosing (always follow your prescription): secondary amenorrhea or abnormal uterine bleeding 5–10 mg once daily for 5–10 days; prevention of endometrial hyperplasia with estrogen 5–10 mg once daily for 12–14 days each month.
Most people have a withdrawal bleed 3–7 days after the last dose; for some it may take up to 2 weeks. If no bleed occurs, contact your clinician to check for pregnancy or other causes.
Bloating, breast tenderness, nausea, headache, dizziness, sleepiness, mood changes, acne or oily skin, mild swelling, and spotting or breakthrough bleeding are common and often improve over time.
Seek urgent care for chest pain, shortness of breath, severe headache, sudden vision changes, one-sided leg swelling/pain (possible clot), jaundice, severe depression, or heavy uncontrolled bleeding.
Avoid if you’re pregnant or suspect pregnancy; have undiagnosed vaginal bleeding, active or past blood clots, stroke or heart attack, significant liver disease, or a history of hormone-sensitive cancer, or a known allergy to medroxyprogesterone.
It is not a contraceptive and does not generally delay return of fertility after you stop. It’s often used short-term to induce a bleed before fertility treatments or to help schedule cycles.
Yes. In PCOS, cyclic Provera can induce regular withdrawal bleeds to protect the endometrium from unopposed estrogen; it does not treat insulin resistance or restore ovulation by itself.
Some clinicians use progestins for short-term period delay, but norethindrone is more commonly chosen. Discuss timing, dosing, and your risk factors before trying this off-label use.
Some people notice fluid retention, appetite changes, or mood shifts. Lifestyle measures can help; if symptoms are significant, ask about dose adjustments or alternative progestins.
Progestin-only pills carry a much lower clot risk than estrogen-containing therapies, but clots are still possible, especially if you have risk factors (smoking, immobility, prior clots). Know warning signs and discuss your history.
CYP3A4 inducers (rifampin, carbamazepine, phenytoin, St. John’s wort) may lower levels; certain antivirals and azoles may raise levels. Always review your full medication list, including herbals.
Take it when you remember unless it’s close to the next dose—then skip the missed dose. Don’t double up. Missing doses can alter timing of the withdrawal bleed.
Progestins are generally compatible with lactation, but timing matters postpartum and data for oral medroxyprogesterone are limited; many clinicians prefer other progestin-only options (e.g., norethindrone) after milk supply is established.
Light alcohol has no known direct interaction, but smoking increases cardiovascular risk with any hormone therapy. Avoid smoking and keep alcohol moderate.
Bleeding often lightens within a few days of starting; full control may take the full course. If bleeding is very heavy (soaking pads hourly), seek urgent care.
Progestins can suppress endometrial tissue activity and reduce pain. Higher-dose or long-acting progestins are more often used; ask your clinician which option fits your goals.
Progestins may slightly worsen insulin resistance and lipid profiles in some people; diabetics should monitor glucose more closely and share results with their clinician.
Provera is an oral tablet used cyclically for bleeding disorders; Depo-Provera is a 3‑month contraceptive injection that strongly suppresses ovulation. The injection is contraceptive and may delay return to fertility; the tablet is not contraceptive.
Both are effective. Norethindrone is sometimes preferred for period delay and has slightly different side-effect profiles (more androgenic effects like acne in some). Choice depends on your history, goals, and tolerability.
Prometrium is bioidentical progesterone, often used for HRT with estrogen and for luteal support; it may cause more sedation and requires peanut-free formulations for some. Provera is a synthetic progestin with robust endometrial protection and tends to be less sedating.
Both protect the endometrium and regulate cycles. Some data suggest dydrogesterone may have a more favorable mood and lipid profile in certain patients, while Provera has wider availability and long clinical experience. Local approval and cost often drive choice.
The LNG-IUD delivers progestin directly to the uterus, often reducing bleeding by 70–90% and providing contraception for years with fewer systemic effects. Provera works while you take it but doesn’t provide contraception and may cause more systemic side effects.
Combined pills regulate cycles and provide contraception but carry higher clot risk due to estrogen. Provera is progestin-only and typically used short term; it’s better for those avoiding estrogen but it won’t prevent pregnancy.
No. Both are progestins, but Megace is used primarily for appetite stimulation and certain cancers at higher doses. Provera is used for gynecologic indications at lower doses. They are not substitutes.
Injections provide continuous ovulation suppression and steady symptom control, but can cause irregular bleeding and delay fertility return; tablets offer flexible, short-term courses but may be less potent for pain control.
Vaginal progesterone delivers high uterine levels with fewer systemic effects and is preferred for luteal support in fertility care. Provera is not typically used for luteal support in assisted reproduction.
The implant is a highly effective contraceptive that can reduce dysmenorrhea but may cause irregular spotting. Provera can schedule a predictable withdrawal bleed but offers no contraception and works only while taken.
Norethindrone POPs prevent pregnancy when taken daily at the same time; Provera tablets for bleeding are not contraceptives. If contraception is desired, a POP or another contraceptive method is needed.
Dydrogesterone or micronized progesterone are more commonly used where approved; Provera is generally not first-line in early pregnancy support. Management should be individualized by a specialist.