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Buy Propecia

KwikMed Only Prescribes and Ships Genuine Merck Propecia® ORDER NOW

Buy Propecia® Online

Learn More About Propecia®
Follow these simple steps to buy Propecia® online:
  1. Select a quantity from the list below.
  2. Log in or register quickly and confidentially.
  3. Complete the free consultation.
  4. Checkout securely using your credit card.

Upon checkout, your Propecia® order will be reviewed by a KwikMed Physician. If approved, your credit card will be charged (or payment confirmed) and your Propecia® will be shipped in confidential packaging via FedEx or USPS. An adult signature is required upon delivery.

Online Propecia® orders are typically reviewed within 4 hours.

Potency Quantity Special Notes U.S. Price Order
1 mg 30 Tablets No Consult Fee! $218.00
1 mg 90 Tablets No Consult Fee! $512.00
1 mg 180 Tablets No Consult Fee! $836.00
1 mg 270 Tablets No Consult Fee! $1169.00
Try Generic Propecia - only $230 for 90 tablets!
Learn More

Shipping Options

FedEx Next Day - Arrives the next business day after physician approval.
Friday orders are delivered on Monday.
Saturday delivery - Contact Customer Service, additional charges may apply.

FedEx Priority - Arrives in 2 business days (AK, HI, PR, GU and VI only).

FedEx Express Saver - Arrives in three business days.

USPS Express Mail - Arrives in 1-2 business days depending on location.

USPS Priority Mail - Arrives in 3-5 business days depending on location.

Orders which complete the physician consultation by 1:00pm Mountain, Monday - Friday will be shipped that same day.

Adult signature required upon delivery for all Propecia® packages.
Packages may be held for pick-up at any FedEx location.
*Please note that only the 30 pill quantity is available for patients shipping to Japan or Australia.

Online Consultation - there is no fee for this consultation

Accurate information is required before any Physician can write a prescription for any illness or condition. A U.S. licensed Physician will review your online consultation and either approve or decline your prescription for Propecia®. If you are declined there will be no charge to you. If you are approved, you will be charged only for the cost of the Propecia® and its associated shipping fee, there are no hidden costs.

How to take Propecia®

Follow your physician's directions when taking Propecia®. If you have any questions regarding Propecia®, talk to your physician, pharmacist or nurse before starting this medication. Propecia® may be taken on an empty stomach once daily. Never take two doses at once.

Side Effects

Propecia® may cause a change in sexual function. If this change becomes bothersome, or does not go away, contact your physician. Contact your physician immediately if you experience swollen lips or a skin rash as these may be signs of toxicity. If you notice any other unusual symptoms contact your physician and inform them that you have been taking Propecia®.

Precautions

Propecia® requires ongoing treatment over several months in order to work. Check with your prescriber before you stop taking this medication. If you stop taking Propecia®, your original state of baldness will return within one year. Be sure to keep all laboratory and physician appointments throughout the course of your treatment. Always contact your physician or pharmacist before taking any prescription or over the counter medication. Women who are, or may become, pregnant are to avoid handling broken or crushed Propecia® tablets. If this contact occurs contact your physician as soon as possible.

Drug Interactions

Inform your physician of all prescription and over the counter medication that you may take. This is especially important with nitrate medications (ex: isosorbide dinitrate and nitroglycerin), azole antifungals (ex: ketoconazole and itraconazole), nitroprusside (which are medicines considered to be "nitric oxide donors"), erythromycin, cimetidine, rifampin (ex: rifampin), medicines for high blood pressure or mibefradil.

Missed Dose

Never take two doses of Propecia® at once. If a dose is missed, skip that dose and take Propecia® and resume your regular Propecia® dosing schedule.

Storing Propecia®

Keep Propecia® at room temperature, 59 - 86 degrees Fahrenheit (15 - 30 degrees Celsius), and stored it in a dry place away from moisture and light. Discard any unused or expired medication in a safe place and always keep prescription drugs out of children's reach.

Notice

Never share Propecia®, or other prescription medication, with others and only use if for the health condition for which it was prescribed. When taking Propecia®, be sure to refill your prescription regularly to avoid running out of tablets and interrupting your treatment.


IMPORTANT SAFETY INFORMATION

INDICATION AND USAGE OF PROPECIA

PROPECIA® is indicated for the treatment of male pattern hair loss (androgenetic alopecia) in MEN ONLY.

Efficacy in bitemporal recession has not been established.

PROPECIA is not indicated for use in women.

DOSAGE AND ADMINISTRATION

PROPECIA may be administered with or without meals.

The recommended dose of PROPECIA is one tablet (1 mg) taken once daily.

In general, daily use for three months or more is necessary before benefit is observed. Continued use is recommended to sustain benefit, which should be re-evaluated periodically. Withdrawal of treatment leads to reversal of effect within 12 months.

CONTRAINDICATIONS

  • Pregnancy. Finasteride use is contraindicated in women when they are or may potentially be pregnant. Because of the ability of Type II 5α-reductase inhibitors to inhibit the conversion of testosterone to 5α-dihydrotestosterone (DHT), finasteride may cause abnormalities of the external genitalia of a male fetus of a pregnant woman who receives finasteride. If this drug is used during pregnancy, or if pregnancy occurs while taking this drug, the pregnant woman should be apprised of the potential hazard to the male fetus.  In female rats, low doses of finasteride administered during pregnancy have produced abnormalities of the external genitalia in male offspring.
  • Hypersensitivity to any component of this medication.

WARNINGS AND PRECAUTIONS

Exposure of Women — Risk to Male Fetus

PROPECIA is not indicated for use in women. Women should not handle crushed or broken PROPECIA tablets when they are pregnant or may potentially be pregnant because of the possibility of absorption of finasteride and the subsequent potential risk to a male fetus. PROPECIA tablets are coated and will prevent contact with the active ingredient during normal handling, provided that the tablets have not been broken or crushed. 

Effects on Prostate Specific Antigen (PSA)

In clinical studies with PROPECIA (finasteride, 1 mg) in men 18-41 years of age, the mean value of serum prostate specific antigen (PSA) decreased from 0.7 ng/mL at baseline to 0.5 ng/mL at Month 12. Further, in clinical studies with PROSCAR (finasteride, 5 mg) when used in older men who have benign prostatic hyperplasia (BPH), PSA levels are decreased by approximately 50%. Other studies with PROSCAR showed it may also cause decreases in serum PSA in the presence of prostate cancer. These findings should be taken into account for proper interpretation of serum PSA when evaluating men treated with finasteride. Any confirmed increase from the lowest PSA value while on PROPECIA may signal the presence of prostate cancer and should be evaluated, even if PSA levels are still within the normal range for men not taking a 5α-reductase inhibitor. Non-compliance to therapy with PROPECIA may also affect PSA test results.

Increased Risk of High-Grade Prostate Cancer with 5α-Reductase Inhibitors

Men aged 55 and over with a normal digital rectal examination and PSA ≤3.0 ng/mL at baseline taking finasteride 5 mg/day (5 times the dose of PROPECIA) in the 7-year Prostate Cancer Prevention Trial (PCPT) had an increased risk of Gleason score 8-10 prostate cancer (finasteride 1.8% vs placebo 1.1%). Similar results were observed in a 4-year placebo-controlled clinical trial with another 5α-reductase inhibitor (dutasteride, AVODART) (1% dutasteride vs 0.5% placebo). 5α-reductase inhibitors may increase the risk of development of high-grade prostate cancer. Whether the effect of 5α-reductase inhibitors to reduce prostate volume, or study-related factors, impacted the results of these studies has not been established.

Pediatric Patients

PROPECIA is not indicated for use in pediatric patients.

ADVERSE REACTIONS / SIDE EFFECTS

The following adverse reactions have been identified during post approval use of PROPECIA. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure:

Hypersensitivity Reaction: hypersensitivity reactions such as rash, pruritus, urticaria, and angioedema (including swelling of the lips, tongue, throat, and face);

Reproductive System: sexual dysfunction that continued after discontinuation of treatment, including erectile dysfunction, libido disorders, ejaculation disorders, and orgasm disorders; male infertility and/or poor seminal quality (normalization or improvement of seminal quality has been reported after discontinuation of finasteride); testicular pain. 

Neoplasms: male breast cancer;

Breast disorders: breast tenderness and enlargement;

Nervous System/Psychiatric: depression

Please see full prescribing information here.

To report SUSPECTED ADVERSE REACTIONS, call 1-855-888-2467 or report via the FDA MedWatch Program at www.fda.gov/medwatch or 1-800-FDA-1088.

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