This site requires JavaScript to be enabled to work properly. Please modify your settings or use a different browser to continue

      

You are now leaving GSK’s website

You are now leaving a GSK Website. By clicking this link, you will be taken to a website that is not owned or controlled by GSK, and GSK is not responsible for the content provided on that site.

Continue

Go back

Products

Anoro Ellipta
(umeclidinium/vilanterol inhalation powder)

Arexvy
(Respiratory Syncytial Virus vaccine recombinant, adjuvanted)

Avamys
(fluticasone furoate)

Dovato
(dolutegravir/lamivudine)

Ellipta inhaler

Imigran
(sumatriptan)

Incruse Ellipta
(umeclidinium bromide)

Nucala
(mepolizumab)

Omjjara
(momelotinib)

Relvar Ellipta
(fluticasone furoate/vilanterol)

Rotarix
(rotavirus vaccine)

Shingrix
Herpes zoster vaccine (recombinant, adjuvanted)

Tivicay
(dolutegravir)

Trelegy Ellipta
(fluticasone furoate/umeclidinium/vilanterol)

Triumeq
(dolutegravir/abacavir/lamivudine)

Vocabria▼ Film-Coated Tablets
(cabotegravir)

Vocabria▼ Suspension for Injection
(cabotegravir) | VOCABRIA (cabotegravir) prolonged-release suspension for injection should always be prescribed with REKAMBYS▼ (rilpivirine long acting). REKAMBYS▼, including trademark, is owned by Janssen Pharmaceutical Companies and used under license by the ViiV Healthcare Group of Companies. Full prescribing information is available at www.ema.europa.eu

Volibris
(ambrisentan)

Zyban
(bupropion hydrochloride)

Zejula
(niraparib tosylate monohydrate)
oncology

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.

These medicinal products are subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

Trade marks are owned by or licensed to the GSK group of companies.