Location via proxy:   [ UP ]  
[Report a bug]   [Manage cookies]                

Dolutegravir/rilpivirine

This is an old revision of this page, as edited by Whywhenwhohow (talk | contribs) at 19:05, 25 March 2020 (create). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)

Dolutegravir/rilpivirine, sold under the brand name Juluca, is a fixed dose combination of antiretroviral drugs for the treatment of HIV/AIDS.[3] It contains the medicines dolutegravir and rilpivirine.[3] It is taken by mouth daily with food.[3]

Dolutegravir/rilpivirine
Combination of
DolutegravirHIV integrase strand transfer inhibitor (INSTI)
RilpivirineHIV nonnucleoside reverse transcriptase inhibitor (NNRTI)
Clinical data
Trade namesJuluca
AHFS/Drugs.comMonograph
License data
Pregnancy
category
Routes of
administration
By mouth
ATC code
Legal status
Legal status
  • UK: POM (Prescription only)[2]
  • US: ℞-only
  • In general: ℞ (Prescription only)
Identifiers
CAS Number
UNII
KEGG

The most common adverse reactions (all grades) are diarrhea and headache.

Dolutegravir/rilpivirine was approved for use in the United States in November 2017[3][4][5] and for use in the European Union in May 2018.[6]

References

  1. ^ a b "Dolutegravir / rilpivirine (Juluca) Use During Pregnancy". Drugs.com. 7 January 2020. Retrieved 25 March 2020.
  2. ^ "Juluca 50 mg/25 mg film-coated tablets - Summary of Product Characteristics (SmPC)". (emc). 25 February 2020. Retrieved 25 March 2020.
  3. ^ a b c d "Juluca- dolutegravir sodium and rilpivirine hydrochloride tablet, film coated". DailyMed. 24 October 2019. Retrieved 25 March 2020.
  4. ^ "Drug Approval Package: Juluca (dolutegravir and rilpivirine)". U.S. Food and Drug Administration (FDA). 29 June 2018. Retrieved 25 March 2020.
  5. ^ "Juluca: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Retrieved 25 March 2020.
  6. ^ "Juluca EPAR". European Medicines Agency (EMA). 11 February 2019. Retrieved 25 March 2020.