MedPath
EMA Approval

Sildenafil Teva

G04BE03

sildenafil

Drugs used in erectile dysfunction

Basic Information

G04BE03

sildenafil

Drugs used in erectile dysfunction

Therapeutic indication

Treatment of men with erectile dysfunction, which is the inability to achieve or maintain a penile erection sufficient for satisfactory sexual performance.

In order for Sildenafil Teva to be effective, sexual stimulation is required.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Sildenafil Teva. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Sildenafil Teva.

Authorisations (1)

EMEA/H/C/001073

Teva B.V.,Teva B.V.,Swensweg 5,2031 GA Haarlem,The Netherlands

Authorised

November 30, 2009

Active Substances (2)

sildenafil

sildenafil

Documents (8)

Sildenafil Teva : EPAR - Public assessment report

December 7, 2009

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Sildenafil Teva : EPAR - Public assessment report

December 7, 2009

CHANGES_SINCE_INITIAL_AUTHORISATION

Committee for medicinal products for human use, summary of positive opinion for Sildenafil Teva

September 23, 2009

CHANGES_SINCE_INITIAL_AUTHORISATION

Sildenafil Teva : EPAR - Summary for the public

December 7, 2009

OVERVIEW_DOCUMENT

Sildenafil Teva : EPAR - All Authorised presentations

December 7, 2009

AUTHORISED_PRESENTATIONS

Sildenafil Teva : EPAR - Procedural steps taken and scientific information after authorisation

May 3, 2010

CHANGES_SINCE_INITIAL_AUTHORISATION

Committee for medicinal products for human use, summary of positive opinion for Sildenafil Teva

September 23, 2009

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Sildenafil Teva : EPAR - Product Information

December 7, 2009

DRUG_PRODUCT_INFORMATION

Overview Q&A (8)

Question

Other information about Sildenafil Teva

Answer

The European Commission granted a marketing authorisation valid throughout the European Union for Sildenafil Teva on 30 November 2009.

For more information about treatment with Sildenafil Teva, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Question

What are the benefits and risks of Sildenafil Teva?

Answer

Because Sildenafil Teva is a generic medicine and is bioequivalent to the reference medicine, its benefits and risks are taken as being the same as the reference medicine’s.

Question

What is Sildenafil Teva used for?

Answer

Sildenafil Teva is used to treat adult men with erectile dysfunction (sometimes called impotence), when they cannot get or keep a hard penis (erection) sufficient for satisfactory sexual activity. For Sildenafil Teva to be effective, sexual stimulation is required.

The medicine can only be obtained with a prescription.

Question

How is Sildenafil Teva used?

Answer

The recommended dose of Sildenafil Teva is 50 mg taken as needed about one hour before sexual activity. If Sildenafil Teva is taken with food, the onset of activity may be delayed compared with taking Sildenafil Teva without food. The dose may be increased to a maximum of 100 mg or decreased to 25 mg depending on the effectiveness and side effects. Patients with liver problems or severe kidney problems should start treatment with the 25 mg dose. The maximum recommended dosing frequency is one tablet per day.

Question

What is Sildenafil Teva?

Answer

Sildenafil Teva is a medicine that contains the active substance sildenafil. It is available as tablets (25, 50 and 100 mg).

Sildenafil Teva is a ‘generic medicine’. This means that Sildenafil Teva is similar to a ‘reference medicine’ already authorised in the European Union (EU) called Viagra.

Question

How does Sildenafil Teva work?

Answer

The active ingredient in Sildenafil Teva, sildenafil, belongs to a group of medicines called phosphodiesterase-type-5 (PDE5) inhibitors. It works by blocking the phosphodiesterase enzyme, which normally breaks down a substance known as cyclic guanosine monophosphate (cGMP). During normal sexual stimulation, cGMP is produced in the penis, where it causes the muscle in the spongy tissue of the penis (the corpora cavernosa) to relax. This allows blood to flow into the corpora, producing the erection. By blocking the breakdown of cGMP, Sildenafil Teva restores erectile function. Sexual stimulation is still needed to produce an erection.

Question

Why has Sildenafil Teva been approved?

Answer

The CHMP concluded that, in accordance with EU requirements, Sildenafil Teva has been shown to have comparable quality and to be bioequivalent to Viagra. Therefore, the CHMP’s view was that, as for Viagra, the benefit outweighs the identified risk. The Committee recommended that Sildenafil Teva be given marketing authorisation.

Question

How has Sildenafil Teva been studied?

Answer

Because Sildenafil Teva is a generic medicine, studies in patients have been limited to tests to determine that it is bioequivalent to the reference medicine, Viagra. Two medicines are bioequivalent when they produce the same levels of the active substance in the body.

© Copyright 2025. All Rights Reserved by MedPath