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Propecia

Propecia is in a class of medications called 5-alpha reductase inhibitors. Propecia treats male pattern hair loss by blocking the body's production of a male hormone in the scalp that stops hair growth.

Other names for this medication:
Astifine, Curlzfin, Finabald, Finap, Finara, Finarid, Finast, Finastat, Finasteride, Finax, Fincar, Findor, Finflow, Finpecia, Finster, Fintec, Fintride, Firide, Fistide, Grohair, Growvita, Gzlfine, Prohair, Proscar, Tampace, Urimax

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Also known as: Finasteride

Description

Propecia is produced by Merck S&D. Propecia treats the most common type of hair loss in mencalled MPHL or MPB (male pattern baldness). It is also known as androgenetic alopecia (AGA). It affects about 50% of men over the age of 50. It is a condition, where hair follicles are being destroyed by the high levels of sex hormone dihydrotestosterone (DHT). DHT binds to androgen receptors in susceptible hair follicles and activates genes responsible for follicular miniaturization. The active ingredient Finasteride is a type II 5-alpha reductase inhibitor and has a trichogenic activity (hair growth-promoting). It hinders the action of 5-alpha reductase enzyme, responsible for the conversion of testosterone to dihydrotestosterone (DHT). Due to inhibiting of this enzyme, Propecia lowers scalp and serum DHT concentrations (up to 60%) and slows down the complete hair loss process. Finasteride in higher doses (Finast, Fincar, Proscar, Prosteride) is used for the treatment and maintenance of benign prostatic hyperplasia (BPH), female hirsutism (in adult, non-pregnant women with PCOS or with idiopathic hirsutism).

Dosage

Take Propecia exactly as prescribed by your doctor. Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.

Take this medicine with a full glass of water.

Propecia can be taken with or without food. Take the medicine at the same time each day.

It is important to use Propecia regularly to get the most benefit. You may need to take Propecia daily for three months or more before you see a benefit. Propecia can only work over the long term if you continue taking it. If the drug has not worked for you in twelve months, further treatment is unlikely to be of benefit. If you stop taking Propecia, you will likely lose the hair you have gained within 12 months of stopping treatment. You should discuss this with your doctor.

To be sure this medication is helping your condition and not causing harmful effects, your blood may need to be tested often. Your doctor will also test your prostate specific antigen (PSA) to check for prostate cancer. Visit your doctor regularly.

Store Propecia at room temperature away from moisture, heat, and light. Keep the bottle tightly closed when not in use.

Detailed Propecia dosage information

Overdose

If an overdose occurs and you are feeling unwell, you should seek emergency medical attention or contact your healthcare provider immediately.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) and away from excess moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Propecia are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not use Propecia if you are allergic to its ingredients or allergic to a similar medication called Dutasteride. Propecia tablets are not indicated for use in women and children. Women must not handle crushed or broken Propecia tablets during pregnancy or lactation, as Finasteride can be absorbed through the skin and cause hypospadias in a male fetus. Be careful while using Propecia if you have liver disease, undergo prostate-specific antigen assay or if you notice breast enlargement and tenderness. Consult a doctor before using Propecia if you have prostate cancer, a bladder muscle disorder, a bladder infection. Consult a doctor before using Propecia if you have narrowing or a blockage in the urinary tract, severe trouble urinating, or if you are unable to urinate. Consult a doctor before using Propecia if you are taking any prescription or nonprescription medications, herbal preparation, or dietary supplement.

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In therapy, NPs may allow more effective cellular and subcellular targeting of drugs. There is some evidence that low-GI foods improve insulin sensitivity in humans, although studies using established techniques (glucose clamp or frequently sampled intravenous glucose tolerance test) have not been done. Changes in carbohydrate and amino acid metabolism in dog brain in experimental alloxan diabetes. In the first experiment, daily footshock stress did not significantly alter the avoidance of Form. Doxepin Mitigates Noise-induced Neuronal Damage in Primary Auditory Cortex of Mice via Suppression of Acid Sphingomyelinase/Ceramide Pathway. In nature, and particularly in the hospital, bacteria that contain beta-lactamases encounter simultaneous or consecutive selective pressure with different beta-lactam molecules. Antioxidant effect of alpha-tocopherol on fracture haematoma in rabbits.

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The neural stimulator system produces biphasic pulses that deliver balanced charge into tissue from single or multichannel electrodes. Electrochemical Dissolution of Iridium and Iridium Oxide Particles in Acidic Media: Transmission Electron Microscopy, Electrochemical Flow Cell Coupled to Inductively Coupled Plasma Mass Spectrometry, and X-ray Absorption Spectroscopy Study. Examining conspiracist beliefs about the disappearance of Amelia Earhart. Module one ensures that equipment needed for treating burn injuries is available to emergency providers. Consistent with a critical role for NTF2 in establishing and maintaining the Ran gradient, we show that NTF2 is required for early embryogenesis in Caenorhabditis elegans. Serum drug concentration was determined by use of a microbiological assay, and the following kinetic values were estimated for each dog: area under the concentration-time curve, peak serum drug concentration (Cmax), time of Cmax, absorption half-life, and elimination half-life (t1/2el). In an attempt to define the possible role of corticotropin-releasing hormone (CRH) on lipopolysaccharide (LPS)-induced type I interleukin-1 receptor (IL-1R1), IL-1alpha, and IL-1beta mRNAs in the pituitary, adrenal gland and spleen, we used CRH-deficient (knockout, KO) mouse in this study. Hepatic stellate cells were freshly isolated from normal human livers (quiescent hepatic stellate cells) and from human cirrhotic livers (in vivo activated hepatic stellate cells). This is especially important as it occurs in young women where fertility considerations must be part of the discussion of any pelvic surgery.

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