Phytodolor--effects and efficacy of a herbal medicine.
Identifieur interne : 003A97 ( Main/Exploration ); précédent : 003A96; suivant : 003A98Phytodolor--effects and efficacy of a herbal medicine.
Auteurs : Karl-Josef Gundermann [Pologne] ; Jürgen MüllerSource :
- Wiener medizinische Wochenschrift (1946) [ 0043-5341 ] ; 2007.
Descripteurs français
- KwdFr :
- Animaux (MeSH), Antirhumatismaux (administration et posologie), Antirhumatismaux (usage thérapeutique), Essais contrôlés randomisés comme sujet (MeSH), Extraits de plantes (administration et posologie), Extraits de plantes (pharmacologie), Extraits de plantes (usage thérapeutique), Humains (MeSH), Modèles animaux de maladie humaine (MeSH), Méthode en double aveugle (MeSH), Phytothérapie (MeSH), Rats (MeSH), Rhumatismes (traitement médicamenteux), Sécurité (MeSH).
- MESH :
- administration et posologie : Antirhumatismaux, Extraits de plantes.
- pharmacologie : Extraits de plantes.
- traitement médicamenteux : Rhumatismes.
- usage thérapeutique : Antirhumatismaux, Extraits de plantes.
- Animaux, Essais contrôlés randomisés comme sujet, Humains, Modèles animaux de maladie humaine, Méthode en double aveugle, Phytothérapie, Rats, Sécurité.
English descriptors
- KwdEn :
- Animals (MeSH), Antirheumatic Agents (administration & dosage), Antirheumatic Agents (therapeutic use), Disease Models, Animal (MeSH), Double-Blind Method (MeSH), Humans (MeSH), Phytotherapy (MeSH), Plant Extracts (administration & dosage), Plant Extracts (pharmacology), Plant Extracts (therapeutic use), Randomized Controlled Trials as Topic (MeSH), Rats (MeSH), Rheumatic Diseases (drug therapy), Safety (MeSH).
- MESH :
- chemical , administration & dosage : Antirheumatic Agents, Plant Extracts.
- chemical , pharmacology : Plant Extracts.
- chemical , therapeutic use : Antirheumatic Agents, Plant Extracts.
- drug therapy : Rheumatic Diseases.
- Animals, Disease Models, Animal, Double-Blind Method, Humans, Phytotherapy, Randomized Controlled Trials as Topic, Rats, Safety.
Abstract
UNLABELLED
Herbal antirheumatics are successfully used in painful inflammatory or degenerative rheumatic diseases. One of these herbal medicines is Phytodolor (STW 1), a fixed combination of extracts from aspen leaves and bark (Populus tremula), common ash bark (Fraxinus excelsior), and golden rod herb (Solidago virgaurea). Its effects as well as those of its components have been verified in experimental and human pharmacological investigations. The mode of action of STW 1 includes antiinflammatory, antioedematous, antioxidative and analgesic properties, and it is considered to be broader than that of synthetic antirheumatics. Open clinical studies and randomised, placebo- or verum-controlled double-blind trials, performed in different subtypes of rheumatic diseases, confirm the pharmacological evidence of efficacy, such as by reducing the intake of non-steroidal antiinflammatory drugs (NSAIDs). STW 1 has a high drug safety.
CONCLUSION
Phytodolor (STW 1) is a reasonable alternative to NSAIDs and to cyclooxygenase(COX)-2-inhibitors such as rofecoxib.
DOI: 10.1007/s10354-007-0436-4
PubMed: 17704984
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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qualifier="administration & dosage" xml:lang="en"><term>Antirheumatic Agents</term><term>Plant Extracts</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Plant Extracts</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Antirheumatic Agents</term><term>Plant Extracts</term></keywords><keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr"><term>Antirhumatismaux</term><term>Extraits de plantes</term></keywords><keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Rheumatic Diseases</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Extraits de plantes</term></keywords><keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr"><term>Rhumatismes</term></keywords><keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Antirhumatismaux</term><term>Extraits de plantes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Disease Models, Animal</term><term>Double-Blind Method</term><term>Humans</term><term>Phytotherapy</term><term>Randomized Controlled Trials as Topic</term><term>Rats</term><term>Safety</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Essais contrôlés randomisés comme sujet</term><term>Humains</term><term>Modèles animaux de maladie humaine</term><term>Méthode en double aveugle</term><term>Phytothérapie</term><term>Rats</term><term>Sécurité</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p><b>UNLABELLED</b></p><p>Herbal antirheumatics are successfully used in painful inflammatory or degenerative rheumatic diseases. One of these herbal medicines is Phytodolor (STW 1), a fixed combination of extracts from aspen leaves and bark (Populus tremula), common ash bark (Fraxinus excelsior), and golden rod herb (Solidago virgaurea). Its effects as well as those of its components have been verified in experimental and human pharmacological investigations. The mode of action of STW 1 includes antiinflammatory, antioedematous, antioxidative and analgesic properties, and it is considered to be broader than that of synthetic antirheumatics. Open clinical studies and randomised, placebo- or verum-controlled double-blind trials, performed in different subtypes of rheumatic diseases, confirm the pharmacological evidence of efficacy, such as by reducing the intake of non-steroidal antiinflammatory drugs (NSAIDs). STW 1 has a high drug safety.</p></div><div type="abstract" xml:lang="en"><p><b>CONCLUSION</b></p><p>Phytodolor (STW 1) is a reasonable alternative to NSAIDs and to cyclooxygenase(COX)-2-inhibitors such as rofecoxib.</p></div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">17704984</PMID><DateCompleted><Year>2007</Year><Month>10</Month><Day>09</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0043-5341</ISSN><JournalIssue CitedMedium="Print"><Volume>157</Volume><Issue>13-14</Issue><PubDate><Year>2007</Year></PubDate></JournalIssue><Title>Wiener medizinische Wochenschrift (1946)</Title><ISOAbbreviation>Wien Med Wochenschr</ISOAbbreviation></Journal><ArticleTitle>Phytodolor--effects and efficacy of a herbal medicine.</ArticleTitle><Pagination><MedlinePgn>343-7</MedlinePgn></Pagination><Abstract><AbstractText Label="UNLABELLED">Herbal antirheumatics are successfully used in painful inflammatory or degenerative rheumatic diseases. One of these herbal medicines is Phytodolor (STW 1), a fixed combination of extracts from aspen leaves and bark (Populus tremula), common ash bark (Fraxinus excelsior), and golden rod herb (Solidago virgaurea). Its effects as well as those of its components have been verified in experimental and human pharmacological investigations. The mode of action of STW 1 includes antiinflammatory, antioedematous, antioxidative and analgesic properties, and it is considered to be broader than that of synthetic antirheumatics. Open clinical studies and randomised, placebo- or verum-controlled double-blind trials, performed in different subtypes of rheumatic diseases, confirm the pharmacological evidence of efficacy, such as by reducing the intake of non-steroidal antiinflammatory drugs (NSAIDs). STW 1 has a high drug safety.</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Phytodolor (STW 1) is a reasonable alternative to NSAIDs and to cyclooxygenase(COX)-2-inhibitors such as rofecoxib.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gundermann</LastName><ForeName>Karl-Josef</ForeName><Initials>KJ</Initials><AffiliationInfo><Affiliation>Department of Pharmacology and Toxicology, Chair of Pharmacology, Pomeranian Medical Academy, Szczecin, Poland. gmc-gundermann@web.de</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Müller</LastName><ForeName>Jürgen</ForeName><Initials>J</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType 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IdType="pubmed">1855751</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed><affiliations><list><country><li>Pologne</li></country></list><tree><noCountry><name sortKey="Muller, Jurgen" sort="Muller, Jurgen" uniqKey="Muller J" first="Jürgen" last="Müller">Jürgen Müller</name></noCountry><country name="Pologne"><noRegion><name sortKey="Gundermann, Karl Josef" sort="Gundermann, Karl Josef" uniqKey="Gundermann K" first="Karl-Josef" last="Gundermann">Karl-Josef Gundermann</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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