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Glycopyrronium bromide information


Glycopyrronium bromide
Clinical data
Trade namesRobinul, Cuvposa, Seebri, others
Other namesglycopyrrolate (USAN US)
AHFS/Drugs.comMonograph
MedlinePlusa602014
License data
  • US DailyMed: Glycopyrrolate
Pregnancy
category
  • AU: B2
Routes of
administration
By mouth, intravenous, inhalation, topical, injection, subcutaneous
Drug classAntimuscarinic agent
ATC code
  • A03AB02 (WHO) D11AA01 (WHO) R03BB06 (WHO)
Legal status
Legal status
  • AU: S3 / S4
  • CA: ℞-only[1]
  • UK: POM (Prescription only)
  • US: ℞-only[2][3]
  • EU: Rx-only[4][5][6][7]
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Elimination half-life0.6–1.2 hours
Excretion85% Kidney, unknown amount in the bile
Identifiers
IUPAC name
  • 3-[2-Cyclopentyl(hydroxy)phenylacetoxy]-1,1-dimethylpyrrolidinium bromide
CAS Number
  • 51186-83-5 checkY
  • as cation: 596-51-0
PubChem CID
  • 3494
  • as cation: 11693
IUPHAR/BPS
  • 7459
DrugBank
  • DBSALT001183 checkY
  • as cation: DB00986
ChemSpider
  • 11201
  • as cation: 3374
UNII
  • V92SO9WP2I
  • as cation: A14FB57V1D
KEGG
  • D00540 checkY
  • as cation: D10938
ChEBI
  • CHEBI:90972
ChEMBL
  • ChEMBL1201027 ☒N
  • as cation: ChEMBL1201335
CompTox Dashboard (EPA)
  • DTXSID6023109 Edit this at Wikidata
ECHA InfoCard100.008.990 Edit this at Wikidata
Chemical and physical data
FormulaC19H28BrNO3
Molar mass398.341 g·mol−1
3D model (JSmol)
  • Interactive image
  • as cation: Interactive image
SMILES
  • C[N+]1(CCC(C1)OC(=O)C(C2CCCC2)(C3=CC=CC=C3)O)C.[Br-]

  • as cation: C[N+]1(CCC(C1)OC(=O)C(C2CCCC2)(C3=CC=CC=C3)O)C
InChI
  • InChI=1S/C19H28NO3.BrH/c1-20(2)13-12-17(14-20)23-18(21)19(22,16-10-6-7-11-16)15-8-4-3-5-9-15;/h3-5,8-9,16-17,22H,6-7,10-14H2,1-2H3;1H/q+1;/p-1
  • Key:VPNYRYCIDCJBOM-UHFFFAOYSA-M

  • as cation: InChI=1S/C19H28NO3/c1-20(2)13-12-17(14-20)23-18(21)19(22,16-10-6-7-11-16)15-8-4-3-5-9-15/h3-5,8-9,16-17,22H,6-7,10-14H2,1-2H3/q+1
  • Key:ANGKOCUUWGHLCE-UHFFFAOYSA-N
 ☒NcheckY (what is this?)  (verify)

Glycopyrronium bromide is a medication of the muscarinic anticholinergic group.[7] It does not cross the blood–brain barrier and consequently has few to no central effects. It is given by mouth,[8] via intravenous injection, on the skin,[9] and via inhalation.[4][5][6] It is a synthetic quaternary ammonium compound.[2] The cation, which is the active moiety, is called glycopyrronium (INN)[10] or glycopyrrolate (USAN).

The most common side effects include irritability, flushing, blocked nose, reduced secretions in the airways, dry mouth, constipation, diarrhea, vomiting and inability to completely empty the bladder (urinary retention).[7]

In September 2012, glycopyrronium was approved for medical use in the European Union.[4] In June 2018, glycopyrronium was approved by the US Food and Drug Administration (FDA) to treat excessive underarm sweating, becoming the first drug developed specifically to reduce excessive sweating.[11] It is on the World Health Organization's List of Essential Medicines.[12]

  1. ^ "Neurological therapies". Health Canada. 9 May 2018. Retrieved 13 April 2024.
  2. ^ a b "Robinul- glycopyrrolate tablet Robinul Forte- glycopyrrolate tablet". DailyMed. 1 June 2021. Retrieved 20 June 2022.
  3. ^ "Dartisla ODT- glycopyrrolate orally disintegrating tablets tablet, orally disintegrating". DailyMed. 9 December 2021. Retrieved 20 June 2022.
  4. ^ a b c Cite error: The named reference Seebri Breezhaler EPAR was invoked but never defined (see the help page).
  5. ^ a b Cite error: The named reference Tovanor Breezhaler EPAR was invoked but never defined (see the help page).
  6. ^ a b Cite error: The named reference Enurev Breezhaler EPAR was invoked but never defined (see the help page).
  7. ^ a b c "Sialanar EPAR". European Medicines Agency. 17 September 2018. Retrieved 29 January 2023. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  8. ^ "Glycopyrrolate Oral Inhalation". MedlinePlus. Archived from the original on 17 August 2021. Retrieved 20 June 2022.
  9. ^ "Glycopyrronium Topical". MedlinePlus. Archived from the original on 17 August 2021. Retrieved 20 June 2022.
  10. ^ Bajaj V, Langtry JA (July 2007). "Use of oral glycopyrronium bromide in hyperhidrosis". The British Journal of Dermatology. 157 (1): 118–121. doi:10.1111/j.1365-2133.2007.07884.x. PMID 17459043. S2CID 29080876.
  11. ^ "FDA OKs first drug made to reduce excessive sweating". AP News. Archived from the original on 2018-07-02. Retrieved 2018-07-02.
  12. ^ World Health Organization (2021). World Health Organization model list of essential medicines: 22nd list (2021). Geneva: World Health Organization. hdl:10665/345533. WHO/MHP/HPS/EML/2021.02.

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