Yiɣi chaŋ yɛligu maŋamaŋa puuni

Tretinoin

Diyila Dagbani Wikipedia
Tɛmplet:Infobox drug/title
Names
PronunciationSee pronunciation note
Trade namesVesanoid, Avita, Renova, others
Clinical data
WHO AWaReScript error: No such module "WDfetch".
Pregnancy
category
Tɛmplet:Infobox drug/pregnancy category
Routes of
use
Topical, by mouth
Defined daily doseNot established[1]
External links
AHFS/Drugs.comSystemic: Tɛmplet:Drugs.com
Topical: Tɛmplet:Drugs.com
MedlinePlusa608032
Legal
[[Regulation of therapeutic goods |Tɛmplet:Engvar data]]Tɛmplet:Infobox drug/licence
Legal statusTɛmplet:Infobox drug/legal status
Pharmacokinetics
Protein binding> 95%
Elimination half-life0.5-2 hours
Identifiers
CAS Number
PubChem CID
PubChem SID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
NIAID ChemDB
PDB ligand
CompTox Dashboard (EPA)
ATC code
Chemical and physical data
FormulaTɛmplet:Infobox drug/chemical formula
Molar massTɛmplet:Chem molar mass
3D model (JSmol)
Melting point180 °C (356 °F)

Tɛmplet:Infobox drug/maintenance categories

Tretinoin, bɛ lahi mi tila shɛli all-trans retinoic acid (ATRA), nyɛla tila shɛli din tibiri ningbuŋ bin tɔra din nye acne la, nti pahi acute promyelocytic leukemia din nye ʒim doro la.[2][3][4] Di kana ningbuŋ bin tɔra din nye acne la, tibbu polo, bɛ mali mi m ʒɛri ningbuŋ maa ka mani kpam ni ʒƐri shɛm.[4]

  1. WHOCC - ATC/DDD Index.
  2. Tretinoin. The American Society of Health-System Pharmacists.
  3. Tivnan, Amanda (2016). Resistance to Targeted Therapies Against Adult Brain Cancers. Springer. p. 123. ISBN 9783319465050. Archived from the original on 2017-11-05. Retrieved 2016-12-20.
  4. 1 2 British national formulary : BNF 69 (69 ed.). British Medical Association. 2015. pp. 627, 821–822. ISBN 9780857111562.