GSKpro for UK healthcare professionals
Ordering and delivery
DECTOVA▼
Report a possible side effect | GSKpro
Request a contact
AREXVY▼
This summer, how can GSK help you deliver the non-seasonal shingles National Immunisation Programme?
Respiratory
Immunocompromised Clinical Data | SHINGRIX
GSKpro Efficacy | SHINGRIX
GSKpro Safety | SHINGRIX
Ellipta critical error studies in COPD
XEVUDY ▼ (sotrovimab)
ZEJULA
OMJJARA▼
Therapy areas | GSKpro UK
Nucala (mepolizumab) Safety
Efficacy | Nucala (mepolizumab)
Burden of disease landing page
Nucala (mepolizumab) Home UK
BLENREP▼
COPD Guidelines
Contact | GSKpro UK
IMT Guidelines
Discontinued products | GSK Pro
GSKpro Impact of Shingles | SHINGRIX
Vaccines
Resources | GSKpro
Relvar Ellipta (fluticasone furoate/vilanterol)
JEMPERLI ▼
Webinars & events | GSKpro
GSK Trelegy – Homepage
Coming soon | GSKpro
ICS/LABA
GSKpro Home | SHINGRIX
Webinars & events | GSKpro
GSKpro Implementation | SHINGRIX (Herpes Zoster vaccine recombinant, adjuvanted)
GSKpro Patient Referrals | SHINGRIX
GSK Trelegy - Comparative Effectiveness Study
Nucala (mepolizumab) Expert Perspectives UK
Immunocompromised | SHINGRIX
Supply
Second Dose
GSKpro SHINGRIX overview | SHINGRIX
Multiple myeloma second-line treatment outcomes | GSK UK
BLENREP▼ (belantamab mafodotin) | GSK UK
BLENREP▼ + Vd: Clinical trial efficacy & safety data | GSK UK
BLENREP▼ (belantamab mafodotin) MoA | GSK UK
DREAMM-7 BLENREP▼ (belantamab mafodotin) Trial | GSK UK
BLENREP▼ (belantamab mafodotin) dosing can be delayed, reduced, or discontinued as part of a strategy to manage side effects
BLENREP▼ Dosing and administration | GSK UK
BLENREP▼ (belantamab mafodotin) resources
Supporting patients on BLENREP▼
BLENREP + Pd: Clinical trial efficacy & safety data | GSK UK
DREAMM-8 BLENREP▼ (belantamab mafodotin) Trial | GSK UK
BLENREP▼ (belantamab mafodotin) news and updates | GSK UK
The multiple myeloma experts | GSK UK
Products | GSKpro
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Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/ or search for MHRA Yellowcard in the Google Play or Apple App store. Adverse events should also be reported to GlaxoSmithKline on 0800 221 441.