Proscar order canada

Forum Title: Proscar Finasteride Users Tips & Tips

NickName123:Hi everyone! I'm looking at some information about finasteride. I'm curious about how often users might encounter this. Is it safe to share these tips/means with anyone?

DoctorSutra:Absolutely! I understand some users might not understand these guidelines. However, I don't think it's always wise to discuss these details with them as it's a very personal decision that requires some understanding of a patient's medical history and current medications.

Hakim:Hello DoctorSutra! I'm a medical professional. I believe that there are a lot of options out there, but some might be more appropriate for a specific patient. Here's a brief explanation:

Finasteride is an oral medication that is used to treat an enlarged prostate. It works by blocking the conversion of testosterone to dihydrotestosterone (DHT), a hormone that can shrink prostate tissues. DHT causes shrinkage of the prostate gland, which can contribute to the development of enlarged prostate. It can also shrink the prostate gland and help prevent prostate enlargement and cancer.

Here are some tips for users to consider:

  1. Use finasteride with caution:Patients should be cautious about using finasteride and only use it with a doctor's recommendation. Finasteride is a prescription medication, and you need to consult a healthcare provider before starting treatment.

  2. Monitor for side effects:If you experience any side effects or have concerns about how finasteride interacts with your body, it's best to let your doctor know.

  3. Use caution if you:Have liver or kidney problems, or are pregnant or breastfeeding

  4. Have a history of liver disease:This may indicate a history of liver disease or an allergy to finasteride.

  5. Take other medications:If you are taking any other medications, talk to your doctor before starting finasteride. Some medications, such as alpha-blockers, antifungal medications, and antibiotics, can interact with finasteride and cause adverse effects.

  6. If you have concerns about side effects, it's best to monitor for potential side effects rather than relying solely on the medical information. Keep in mind that finasteride and any other medications that are prescribed by a doctor should be monitored closely for potential side effects.

Thanks so much for this information! I have a lot more questions about the tips for using finasteride, but I thought I would share them here as well. First off, how often does it happen to get a DHT-blocking drug prescribed to you? What's the best time to go for a consultation?

First off, it's important to have an open discussion with a healthcare provider to discuss any concerns or questions you might have about this drug. You should also consult with your doctor to make sure it's safe to start a conversation with you.

Thank you so much for the information! That's really helpful information to have in your thoughts!

I know this dialogue might be helpful, but I've never heard of anyone being on such a med, and I'm wondering if anyone else has experiences with it?

You've given me a lot of great advice, and I'm really glad I did.

Thank you so much for the tip-off! I've never heard of anyone being on such a med, and I'm really hoping my experience here is similar to yours.

You're really good at this kind of information! I'm glad I've found your site helpful. Remember, everyone's unique situation can sometimes have a big impact on understanding their medication options. Always remember that everyone's unique situation can sometimes have a big impact on understanding their medication options.

It's important to do your research and consult a healthcare provider before starting any new medication.

Product description

Product name:PROSCAR®

Company name:

DIN:00594776

Status:Marketed

Status date:2023-01-29

Active ingredient(s)Strength
FINASTERIDE5 MG

Resources

Click on a resource to visit a page with more information. You may be taken away from this page to a different Government of Canada website.

For consumers
ResourceDescription

The Product Monograph is a scientific document that describes the properties, claims, indications and conditions of use of the product and contains any other information that may be required for optimal, safe and effective use.

The Product Monograph includes three sections:

  • Part I: Health Professional Information;
  • Part II: Scientific Information; and
  • Patient Medication Information

Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine.

All suspected side effects should be reported, especially those that are:

  • Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or
  • Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death;
  • Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.
For health care professionals

    Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital.

    This regulatory requirement only applies to hospitals.

    For researchers
      After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.
      All resources

      Objectives:This study aimed to evaluate the effectiveness of the 5-α-reductase inhibitor finasteride (Proscar) and to assess the clinical response in a real-life clinical study. This is a real-life cohort study. A total of 528 patients with benign prostatic hyperplasia (BPH) were enrolled in a real-life clinical study (mean age 71 years, SD 28.4 years). The patients underwent physical examination and an endodontic examination. The patients were diagnosed with BPH by a radiologist. All the patients were randomly assigned to finasteride (5 mg/day) or a placebo group. The primary outcome was the reduction of the total prostate volume in the upper endodontic region (E2, P50) or upper urinary tract (P6). The secondary outcome was the change in urinary flow rate (QRT), which was measured during the period of follow-up. Statistical analysis was performed using the SPSS version 13.0 (SPSS, Chicago, Illinois, USA). The results were statistically significant at the 95% confidence interval. The mean age of the patients in the finasteride group was 71.5 years, which was lower than the age in the placebo group (P= 0.0004). The mean P6 prostate volume in the finasteride group was 9.1 cm3 and 3.2 cm3, respectively (= 0.0003). The mean QRT in the finasteride group was 90.3 mL/min and in the placebo group was 81.4 mL/min (<0.0001). The mean improvement in urinary flow rate (QRT) in the finasteride group was significantly reduced compared with the placebo group (= 0.0079). The mean P6 prostate volume was 9.1 cm3 in the finasteride group and 4.8 cm3 in the placebo group (The mean improvement in urinary flow rate (QRT) was significantly improved in the finasteride group (<0.0001), but it was not statistically significant compared with the placebo group (= 0.26). The mean improvement in urinary flow rate (QRT) in the finasteride group was significantly decreased compared with the placebo group (The mean improvement in urinary flow rate (QRT) was significantly improved in the finasteride group compared with the placebo group (The mean improvement in the urinary flow rate (QRT) in the finasteride group was significantly decreased compared with the placebo group (= 0.13). The mean change in urinary flow rate (QRT) in the finasteride group was significantly decreased compared with the placebo group (= 0.16).

      All the analyzed groups were similar and all patients had a similar response to finasteride.

      Discussion:Finasteride (5 mg/day) has been approved by the FDA for the treatment of benign prostatic hyperplasia. In this study, 5-α-reductase inhibitors were used to treat BPH. Although the results of the study were different, the finasteride group had significantly reduced urinary flow rate (= 0.0079) and QTc reduction (= 0.0089). The finasteride group also demonstrated an improvement in QRT in the E2 and P6, and a significant improvement in urinary flow rate (There was no difference in the change in urinary flow rate between the finasteride and placebo groups (<0.05).

      Conclusion:This study demonstrated that the 5-α-reductase inhibitor finasteride (Proscar) and the placebo group were able to improve the clinical response to finasteride. This finding was statistically significant at the 95% confidence interval. The clinical response was more pronounced in the finasteride group than the placebo group (

      References:

      1.

      A new study suggests that the use of oral finasteride could have serious health risks.

      A new study shows finasteride may cause serious, and potentially fatal, problems in the blood, especially with long-term use. One of the new findings is that the medication may cause a slight increase in the risk of cancer.

      The study was presented at the American College of Cardiology Annual Scientific Session.

      Dr. John S. Lue, of the University of Texas Health Science Center at San Antonio, presented the results at the American College of Cardiology Annual Scientific Session.

      "This is a new study, and it's very important to understand the mechanisms by which finasteride can affect the body," Lue said. "Our preliminary findings suggest that the use of finasteride could have serious health risks for patients taking the medication and potentially also for long-term users."

      The new study, published in the Annals of Internal Medicine, is the first to show that finasteride may cause serious problems in the blood.

      Finasteride is a 5-alpha reductase inhibitor. The medication is not approved for use in the United States. The drug is prescribed for the treatment of male pattern baldness, and is also used to treat enlarged prostate.

      A number of studies have shown that finasteride can cause problems with the kidneys. However, this study shows that it is not likely that finasteride will cause a major health problem. The new study suggests that finasteride may cause serious problems in the blood, especially with long-term use.

      The study was conducted in two sites. Researchers randomly assigned male participants to take the drug either for 5-alpha reductase inhibitors (such as finasteride, Proscar, or Propecia) or finasteride, or placebo.

      Finasteride, known by its brand names Propecia and Proscar, is used to treat male pattern baldness. It is used to treat benign prostatic hyperplasia (BPH), or an enlarged prostate. Propecia is taken once daily.

      Researchers also wanted to test whether the drug could also cause problems with the heart. They also wanted to see if the study results would also be helpful in guiding doctors.

      Previous studies have shown that finasteride can increase the risk of developing a type of breast cancer called breast cancer of the breast. A study published in the British Medical Journal found that finasteride had a similar risk for breast cancer.

      The new study was done on men 18 and older who had been taking finasteride for at least a year.

      The drug was taken once daily for at least three months and then stopped.

      The study was performed in two parts: a follow-up study on the men 18-55 years of age who were taking finasteride for up to six months, and a case-control study on the men 18-59 years of age who were taking finasteride for at least six months.

      The follow-up study was run for over 24 weeks to check if finasteride had caused breast cancer. Results of the study were published in the British Medical Journal in July 2019. The study was funded by Eli Lilly and Company, and the research was funded by the maker of finasteride.

      Researchers then used data from the follow-up study to determine if finasteride was associated with a significant increase in the risk of developing breast cancer.

      The researchers used data from the three groups of men and women they were assigned to take either 5-alpha reductase inhibitors (such as finasteride, Propecia) or finasteride, or placebo.

      They tested the odds of being diagnosed with breast cancer for men 18 and older and women 18-59 years of age, and for men 18-59 years of age who were taking 5-alpha reductase inhibitors. The results showed an increase in the risk of breast cancer in men 18 and over, with a statistically significant increase in the risk of breast cancer in women.

      The researchers also looked at the risk of developing breast cancer in men 18-55 years of age, and women 18-59 years of age. The researchers found an increase in the risk of breast cancer in men 18 and over, with a statistically significant increase in the risk of breast cancer in women.

      The researchers noted that a lower incidence of breast cancer was associated with finasteride use for 5-alpha reductase inhibitors in men. However, there was no evidence of an increased risk for men 18-55 years of age.

      Finasteride is also taken by men who are taking an alpha blocker.