DOLUTEGRAVIR sodium (DTG), eq. 50mg base, tab.

STD DORADOLU5T-

Valid Article

Classification of the medicines in groups and subgroups according to their therapeutic use. The classification used by MSF is based on the WHO Model List of Essential Medicines.
J05AJ03
Anatomical Therapeutic Chemical Classification according to WHOCC
Thermosensitive codes are defined for storage and transportation temperature requirements of the products.
OC subscriptions: included in supply or field order tools (e.g. UniField)
SC subscriptions: included in supply or field tools
OC validations: approved for procurement and use by an OC for international or local orders specifying context and activity in Medical Standard Lists (MSL)

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DOLUTEGRAVIR (DTG)

Therapeutic Action

Antiretroviral, Integrase Strand Transfer Inhibitor (INSTI)

Indications

HIV infection, in combination with other antiretrovirals

Instructions for use

The 10 mg dispersible tablet for oral solution is intended for children from at least 4 weeks old and from 3 to 20 kg:

  • Do not chew or crush the dispersible tablet.
  • Fully disperse in 5 ml of drinking water (for 1 to 3 tab) or 10 ml (for 4, 5 to 6 tablets) in the supplied cup.
  • Swirl the suspension until full dispersion.
  • Give dose to patient. Add again 5 ml of water to the cup to rinse and administer to patient.
  • Administer within 30 minutes of mixing.

In children 20 kg and over, preferably use 50 mg tablet unless they cannot swallow tablets.

When dolutegravir is used in association with other antiretrovirals:

  • In children from 6 to 24.9 kg, a fixed-dose combination (FDC) ABC 60mg / 3TC 30mg / DTG 5mg, disp. tab. is available.
  • In children from 20 to 30 kg, use dolutegravir 50 mg tablet in combination with a fixed-dose combination (FDC) ABC 120mg / 3TC 60mg, disp. breakable tab.
  • In adolescents > 30 kg and adults, a fixed-dose combination (FDC) TDF 300mg / 3TC 300mg / DTG 50mg, tab. is available.

Storage

Below 25ºC - Protect from sunlight - Protect from humidity