Clobutinol: Difference between revisions
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{{ | {{Drugbox | ||
| IUPAC_name | | Verifiedfields = changed | ||
| image | | Watchedfields = changed | ||
| | | verifiedrevid = 447812939 | ||
| | | IUPAC_name = (''RS'')-1-(4-chlorophenyl)-4-dimethylamino-2,3-dimethyl-butan-2-ol | ||
| | | image = clobutinol.png | ||
| width = 240 | |||
| imagename = 1 : 1 mixture (racemate) | |||
| | | drug_name = Clobutinol | ||
| | |||
<!--Clinical data--> | |||
| | | tradename = | ||
| | | Drugs.com = {{drugs.com|international|clobutinol}} | ||
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | |||
| pregnancy_US = <!-- A / B / C / D / X --> | |||
| pregnancy_AU | | pregnancy_category = | ||
| pregnancy_US | | legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> | ||
| pregnancy_category= | | legal_CA = <!-- / Schedule I, II, III, IV, V, VI, VII, VIII --> | ||
| legal_AU | | legal_UK = <!-- GSL / P / POM / CD / Class A, B, C --> | ||
| legal_CA | | legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> | ||
| legal_UK | | legal_status = Withdrawn | ||
| legal_US | <sub>(EU)</sub>| routes_of_administration = oral | ||
| legal_status | |||
| routes_of_administration = | <!--Pharmacokinetic data--> | ||
| bioavailability = | |||
| protein_bound = | |||
| metabolism = | |||
| elimination_half-life = | |||
| excretion = | |||
<!--Identifiers--> | |||
| CAS_number_Ref = {{cascite|correct|??}} | |||
| CAS_number = 14860-49-2 | |||
| ATC_prefix = R05 | |||
| ATC_suffix = DB03 | |||
| PubChem = 26937 | |||
| ChEMBL_Ref = {{ebicite|changed|EBI}} | |||
| ChEMBL = 1474889 | |||
| DrugBank_Ref = {{drugbankcite|changed|drugbank}} | |||
| DrugBank = DB09004 | |||
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | |||
| ChemSpiderID = 25085 | |||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
| UNII = 1NY2IX043A | |||
| KEGG_Ref = {{keggcite|correct|kegg}} | |||
| KEGG = D07716 | |||
<!--Chemical data--> | |||
| C=14 | H=22 | Cl=1 | N=1 | O=1 | |||
| molecular_weight = 255.783 g/mol | |||
| smiles = Clc1ccc(cc1)CC(O)(C)C(C)CN(C)C | |||
| InChI = 1/C14H22ClNO/c1-11(10-16(3)4)14(2,17)9-12-5-7-13(15)8-6-12/h5-8,11,17H,9-10H2,1-4H3 | |||
| InChIKey = KVHHQGIIZCJATJ-UHFFFAOYAE | |||
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | |||
| StdInChI = 1S/C14H22ClNO/c1-11(10-16(3)4)14(2,17)9-12-5-7-13(15)8-6-12/h5-8,11,17H,9-10H2,1-4H3 | |||
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | |||
| StdInChIKey = KVHHQGIIZCJATJ-UHFFFAOYSA-N | |||
}} | }} | ||
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==Side effects and withdrawal== | ==Side effects and withdrawal== | ||
Studies in 2004 had indicated that clobutinol has the potential to prolong the [[QT interval]].<ref name="pmid15280442">{{ cite pmid | 15280442 }}</ref> | |||
Clobutinol was in 2007 determined to cause [[cardiac arrhythmia]] in some patients.<ref> | |||
{{ cite web | |||
| url = http://www.bfarm.de/DE/BfArM/Presse/mitteil2007/pm20-2007.html | |||
| title = Clobutinol-haltige Arzneimittel: BfArM ordnet Widerruf der Zulassung an. | |||
| publisher = BfArM (German Federal Institute for Drugs and Medical Devices) | |||
| date = 2007-08-31 | |||
| quote = Clobutinol: BfArM orders cancellation of approval | |||
}}</ref> | |||
[[Boehringer Ingelheim]] products containing clobutinol were voluntarily withdrawn from sale in [[Germany]], and the rest of the world, on August 31, 2007.<ref> | |||
{{ cite web | |||
| url = http://www.boehringer-ingelheim.com/news/news_releases/press_releases/2007/31_august_2007.html | |||
| publisher = Boehringer Ingelheim | |||
| date = 2007-08-31 | |||
| title = Boehringer Ingelheim voluntarily withdraws its clobutinol containing medications. | |||
}}</ref> | |||
The approval for Germany and the EU was revoked in 2008.<ref> | |||
{{ cite web | |||
| title = Cancellation of approval | |||
| url = http://www.bfarm.de/SharedDocs/1_Downloads/DE/Pharmakovigilanz/stufenplverf/globutinol_bescheid_080613.pdf?__blob=publicationFile | |||
| format = pdf | |||
| quote = Die Zulassungen für die o.g. Arzneimittel werden mit sofortiger Wirkung widerrufen. | |||
| publisher = BfArM (German Federal Institute for Drugs and Medical Devices) | |||
| date = 2008-06-06 | |||
}}</ref> | |||
==See also== | ==See also== | ||
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==References== | ==References== | ||
{{reflist}} | |||
{{ | |||
{{Cough and cold preparations}} | {{Cough and cold preparations}} | ||
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[[Category:Organochlorides]] | [[Category:Organochlorides]] | ||
[[Category:Amines]] | [[Category:Amines]] | ||
[[Category:Alcohols]] | |||
{{respiratory-system-drug-stub}} | |||
{{ |
Revision as of 17:25, 6 April 2015
Clinical data | |
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AHFS/Drugs.com | International Drug Names |
Routes of administration | oral |
ATC code | |
Legal status | |
Legal status |
|
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEMBL | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C14H22ClNO |
Molar mass | 255.783 g/mol |
3D model (JSmol) | |
| |
| |
(what is this?) (verify) |
Clobutinol is a cough suppressant distributed by Boehringer-Ingelheim, Novartis's Hexal (Sandoz), Stada and possibly other companies.
Side effects and withdrawal
Studies in 2004 had indicated that clobutinol has the potential to prolong the QT interval.[1] Clobutinol was in 2007 determined to cause cardiac arrhythmia in some patients.[2]
Boehringer Ingelheim products containing clobutinol were voluntarily withdrawn from sale in Germany, and the rest of the world, on August 31, 2007.[3]
The approval for Germany and the EU was revoked in 2008.[4]
See also
References
- ↑ PMID 15280442 (PMID 15280442)
Citation will be completed automatically in a few minutes. Jump the queue or expand by hand - ↑
"Clobutinol-haltige Arzneimittel: BfArM ordnet Widerruf der Zulassung an". BfArM (German Federal Institute for Drugs and Medical Devices). 2007-08-31.
Clobutinol: BfArM orders cancellation of approval
- ↑ "Boehringer Ingelheim voluntarily withdraws its clobutinol containing medications". Boehringer Ingelheim. 2007-08-31.
- ↑
"Cancellation of approval" (pdf). BfArM (German Federal Institute for Drugs and Medical Devices). 2008-06-06.
Die Zulassungen für die o.g. Arzneimittel werden mit sofortiger Wirkung widerrufen.
Categories:
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