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Safety of Rupatadine Administered Over a Period of 1 Year in the Treatment of Persistent Allergic Rhinitis: A Multicentre Open-Label Study in Spain
Background: Rupatadine (Rupafin®), a novel antihistamine approved recently in Europe for the treatment of allergic rhinitis (AR) and chronic idiopathic urticaria in patients aged ≥12 years, has been shown to be highly efficacious, and as safe and well tolerated as other commonly employed antihistami...
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Published in: | Drug safety 2009, Vol.32 (1), p.33-42 |
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description | Background:
Rupatadine (Rupafin®), a novel antihistamine approved recently in Europe for the treatment of allergic rhinitis (AR) and chronic idiopathic urticaria in patients aged ≥12 years, has been shown to be highly efficacious, and as safe and well tolerated as other commonly employed antihistamines in the treatment of allergic disease. There are, however, few data on the long-term safety of these antihistamines derived in accordance with the clinical safety recommendations of the European Agency for the Evaluation of Medicinal Products (EMEA) and the International Conference on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use Guideline.
Objective:
To assess the safety and tolerability of treatment with rupatadine 10 mg/day for 12 months in subjects with persistent AR (PER).
Methods:
A multicentre, open-label, phase IV study in patients recruited from 33 centres in Spain, from September 2002 to November 2005. The study enrolled 324 male and female patients (aged 12–70 years) with a medical history of PER for at least 12 months and a documented positive skin-prick test to an appropriate allergen. On 4 of the 7 days prior to start of treatment, the patients were required to have a minimum total nasal symptom score (TNSS [for sneezing, rhinorrhoea, nasal obstruction/congestion and nasal itching]) of ≥5. Of the 324 eligible patients starting treatment, 120 needed to be treated for more than 6 months and were followed up until the end of 12 months. All patients received rupatadine 10 mg/day and were allowed to continue their normal concomitant medication for all conditions, other than rhinitis, for up to 6 or 12 months. Safety was assessed by means of adverse events (AEs) reported by patients or detected by investigators, scheduled centralized ECG with special attention to Bazzet corrected QT interval (QTcB) and standard laboratory investigations.
Results:
Assessment of treatment compliance rates indicated 90% and 83% of patients to be compliant during the 1–6 months and 1–12 months treatment periods, respectively, with compliance rates >80% being associated with the majority of the study population reporting at least one AE. Overall, 74.1% and 65.8% of the patients reported at least one AE during the 1–6 months and 1–12 months treatment periods, respectively, compared with 20.4% and 10.8% of patients reporting at least one treatment-related AE during these periods. Disorders of the nervous system and respirator |
doi_str_mv | 10.2165/00002018-200932010-00003 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_20291404</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A222409852</galeid><sourcerecordid>A222409852</sourcerecordid><originalsourceid>FETCH-LOGICAL-c435t-d01195d6fe6b293251c9a1eb4c7dd792f75d1565f33f46e04d71e37b166b11c23</originalsourceid><addsrcrecordid>eNqFkU1v3CAQhq2qVbNN-xcqVKm9OWUAY3NcRf2SIqVK00NPFoZhw8rGW8CV8u-Lu9tE6qVwAIbnHWZ4q4oAvWAgm_e0DEahqxmlipcdrdcQf1JtAFpVgxLsabWhAKJuFMiz6kVK-0J0THbPqzNQwFlH-abaf9MO8z2ZHblZDjpr6wOSrZ188CljREuuf2EkmnzF6Ge7gkB-oI7EB5LvkNxG1HnCkNerAqVVV07bccS484bc3JVc2aeX1TOnx4SvTut59f3jh9vLz_XV9acvl9ur2gje5NqWqlVjpUM5sNJcA0ZpwEGY1tpWMdc2FhrZOM6dkEiFbQF5O4CUA4Bh_Lx6d8x7iPPPBVPuJ58MjqMOOC-pZ5QpEFQU8M0_4H5eYii19YyxtnyrUgW6OEI7PWLvg5tz1KZMi5M3c0DnS3xbBIKqrlmf744CE-eUIrr-EP2k430PtF_d6_-61z-49yfEi_T1qaBlmNA-Ck92FeDtCdDJ6NFFHYxPDxwDoAJaWTh15FK5CjuMj539t4jfuBuwOA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>222720199</pqid></control><display><type>article</type><title>Safety of Rupatadine Administered Over a Period of 1 Year in the Treatment of Persistent Allergic Rhinitis: A Multicentre Open-Label Study in Spain</title><source>Springer Nature</source><creator>Valero, Antonio ; de la Torre, Fernando ; Castillo, José Antonio ; Rivas, Pilar ; del Cuvillo, Alfonso ; Antépara, Ignacio ; Borja, Javier ; Donado, Esther ; Molà, Oriol ; Izquierdo, Iñaki</creator><creatorcontrib>Valero, Antonio ; de la Torre, Fernando ; Castillo, José Antonio ; Rivas, Pilar ; del Cuvillo, Alfonso ; Antépara, Ignacio ; Borja, Javier ; Donado, Esther ; Molà, Oriol ; Izquierdo, Iñaki</creatorcontrib><description>Background:
Rupatadine (Rupafin®), a novel antihistamine approved recently in Europe for the treatment of allergic rhinitis (AR) and chronic idiopathic urticaria in patients aged ≥12 years, has been shown to be highly efficacious, and as safe and well tolerated as other commonly employed antihistamines in the treatment of allergic disease. There are, however, few data on the long-term safety of these antihistamines derived in accordance with the clinical safety recommendations of the European Agency for the Evaluation of Medicinal Products (EMEA) and the International Conference on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use Guideline.
Objective:
To assess the safety and tolerability of treatment with rupatadine 10 mg/day for 12 months in subjects with persistent AR (PER).
Methods:
A multicentre, open-label, phase IV study in patients recruited from 33 centres in Spain, from September 2002 to November 2005. The study enrolled 324 male and female patients (aged 12–70 years) with a medical history of PER for at least 12 months and a documented positive skin-prick test to an appropriate allergen. On 4 of the 7 days prior to start of treatment, the patients were required to have a minimum total nasal symptom score (TNSS [for sneezing, rhinorrhoea, nasal obstruction/congestion and nasal itching]) of ≥5. Of the 324 eligible patients starting treatment, 120 needed to be treated for more than 6 months and were followed up until the end of 12 months. All patients received rupatadine 10 mg/day and were allowed to continue their normal concomitant medication for all conditions, other than rhinitis, for up to 6 or 12 months. Safety was assessed by means of adverse events (AEs) reported by patients or detected by investigators, scheduled centralized ECG with special attention to Bazzet corrected QT interval (QTcB) and standard laboratory investigations.
Results:
Assessment of treatment compliance rates indicated 90% and 83% of patients to be compliant during the 1–6 months and 1–12 months treatment periods, respectively, with compliance rates >80% being associated with the majority of the study population reporting at least one AE. Overall, 74.1% and 65.8% of the patients reported at least one AE during the 1–6 months and 1–12 months treatment periods, respectively, compared with 20.4% and 10.8% of patients reporting at least one treatment-related AE during these periods. Disorders of the nervous system and respiratory thoracic and media-stinal system, in particular headache, somnolence and catarrh, were the three most common AEs reported by >5% of the patients during both treatment periods. Detailed ECG assessments demonstrated no clinically relevant abnormal ECG findings, nor any QTcB increases >60 msec or QTcB values >470 msec for any patient at any time during treatment. Serious AEs were reported in seven patients, of whom six were considered as unlikely to be related to rupatadine treatment, whereas one involving increased blood enzyme levels was considered as possibly related to rupatadine treatment.
Conclusion:
This study confirmed the good long-term safety and tolerability of rupatadine at the therapeutic dose of 10 mg/day in patients with PER.</description><identifier>ISSN: 0114-5916</identifier><identifier>EISSN: 1179-1942</identifier><identifier>DOI: 10.2165/00002018-200932010-00003</identifier><identifier>PMID: 19132803</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adolescent ; Adult ; Aged ; Allergic diseases ; Analysis ; Antihistamines ; Biological and medical sciences ; Child ; Clinical trial. Drug monitoring ; Complications and side effects ; Cyproheptadine - adverse effects ; Cyproheptadine - analogs & derivatives ; Cyproheptadine - therapeutic use ; Development and progression ; Dosage and administration ; Drug Safety and Pharmacovigilance ; Drug therapy ; Electrocardiography ; Female ; Follow-Up Studies ; General pharmacology ; Histamine H1 Antagonists - adverse effects ; Histamine H1 Antagonists - therapeutic use ; Humans ; Immunopathology ; Male ; Medical sciences ; Medication Adherence - statistics & numerical data ; Medicine ; Medicine & Public Health ; Middle Aged ; Non tumoral diseases ; Original Research Article ; Otorhinolaryngology. Stomatology ; Patient compliance ; Patient outcomes ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Respiratory and ent allergic diseases ; Rhinitis ; Rhinitis, Allergic, Perennial - drug therapy ; Spain - epidemiology ; Time Factors ; Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology ; Young Adult</subject><ispartof>Drug safety, 2009, Vol.32 (1), p.33-42</ispartof><rights>Adis Data Information BV 2008</rights><rights>2009 INIST-CNRS</rights><rights>COPYRIGHT 2009 Wolters Kluwer Health, Inc.</rights><rights>Copyright Wolters Kluwer Health Adis International 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c435t-d01195d6fe6b293251c9a1eb4c7dd792f75d1565f33f46e04d71e37b166b11c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21104176$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19132803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Valero, Antonio</creatorcontrib><creatorcontrib>de la Torre, Fernando</creatorcontrib><creatorcontrib>Castillo, José Antonio</creatorcontrib><creatorcontrib>Rivas, Pilar</creatorcontrib><creatorcontrib>del Cuvillo, Alfonso</creatorcontrib><creatorcontrib>Antépara, Ignacio</creatorcontrib><creatorcontrib>Borja, Javier</creatorcontrib><creatorcontrib>Donado, Esther</creatorcontrib><creatorcontrib>Molà, Oriol</creatorcontrib><creatorcontrib>Izquierdo, Iñaki</creatorcontrib><title>Safety of Rupatadine Administered Over a Period of 1 Year in the Treatment of Persistent Allergic Rhinitis: A Multicentre Open-Label Study in Spain</title><title>Drug safety</title><addtitle>Drug-Safety</addtitle><addtitle>Drug Saf</addtitle><description>Background:
Rupatadine (Rupafin®), a novel antihistamine approved recently in Europe for the treatment of allergic rhinitis (AR) and chronic idiopathic urticaria in patients aged ≥12 years, has been shown to be highly efficacious, and as safe and well tolerated as other commonly employed antihistamines in the treatment of allergic disease. There are, however, few data on the long-term safety of these antihistamines derived in accordance with the clinical safety recommendations of the European Agency for the Evaluation of Medicinal Products (EMEA) and the International Conference on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use Guideline.
Objective:
To assess the safety and tolerability of treatment with rupatadine 10 mg/day for 12 months in subjects with persistent AR (PER).
Methods:
A multicentre, open-label, phase IV study in patients recruited from 33 centres in Spain, from September 2002 to November 2005. The study enrolled 324 male and female patients (aged 12–70 years) with a medical history of PER for at least 12 months and a documented positive skin-prick test to an appropriate allergen. On 4 of the 7 days prior to start of treatment, the patients were required to have a minimum total nasal symptom score (TNSS [for sneezing, rhinorrhoea, nasal obstruction/congestion and nasal itching]) of ≥5. Of the 324 eligible patients starting treatment, 120 needed to be treated for more than 6 months and were followed up until the end of 12 months. All patients received rupatadine 10 mg/day and were allowed to continue their normal concomitant medication for all conditions, other than rhinitis, for up to 6 or 12 months. Safety was assessed by means of adverse events (AEs) reported by patients or detected by investigators, scheduled centralized ECG with special attention to Bazzet corrected QT interval (QTcB) and standard laboratory investigations.
Results:
Assessment of treatment compliance rates indicated 90% and 83% of patients to be compliant during the 1–6 months and 1–12 months treatment periods, respectively, with compliance rates >80% being associated with the majority of the study population reporting at least one AE. Overall, 74.1% and 65.8% of the patients reported at least one AE during the 1–6 months and 1–12 months treatment periods, respectively, compared with 20.4% and 10.8% of patients reporting at least one treatment-related AE during these periods. Disorders of the nervous system and respiratory thoracic and media-stinal system, in particular headache, somnolence and catarrh, were the three most common AEs reported by >5% of the patients during both treatment periods. Detailed ECG assessments demonstrated no clinically relevant abnormal ECG findings, nor any QTcB increases >60 msec or QTcB values >470 msec for any patient at any time during treatment. Serious AEs were reported in seven patients, of whom six were considered as unlikely to be related to rupatadine treatment, whereas one involving increased blood enzyme levels was considered as possibly related to rupatadine treatment.
Conclusion:
This study confirmed the good long-term safety and tolerability of rupatadine at the therapeutic dose of 10 mg/day in patients with PER.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Allergic diseases</subject><subject>Analysis</subject><subject>Antihistamines</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Clinical trial. Drug monitoring</subject><subject>Complications and side effects</subject><subject>Cyproheptadine - adverse effects</subject><subject>Cyproheptadine - analogs & derivatives</subject><subject>Cyproheptadine - therapeutic use</subject><subject>Development and progression</subject><subject>Dosage and administration</subject><subject>Drug Safety and Pharmacovigilance</subject><subject>Drug therapy</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>General pharmacology</subject><subject>Histamine H1 Antagonists - adverse effects</subject><subject>Histamine H1 Antagonists - therapeutic use</subject><subject>Humans</subject><subject>Immunopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medication Adherence - statistics & numerical data</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Non tumoral diseases</subject><subject>Original Research Article</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Patient compliance</subject><subject>Patient outcomes</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Respiratory and ent allergic diseases</subject><subject>Rhinitis</subject><subject>Rhinitis, Allergic, Perennial - drug therapy</subject><subject>Spain - epidemiology</subject><subject>Time Factors</subject><subject>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><subject>Young Adult</subject><issn>0114-5916</issn><issn>1179-1942</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v3CAQhq2qVbNN-xcqVKm9OWUAY3NcRf2SIqVK00NPFoZhw8rGW8CV8u-Lu9tE6qVwAIbnHWZ4q4oAvWAgm_e0DEahqxmlipcdrdcQf1JtAFpVgxLsabWhAKJuFMiz6kVK-0J0THbPqzNQwFlH-abaf9MO8z2ZHblZDjpr6wOSrZ188CljREuuf2EkmnzF6Ge7gkB-oI7EB5LvkNxG1HnCkNerAqVVV07bccS484bc3JVc2aeX1TOnx4SvTut59f3jh9vLz_XV9acvl9ur2gje5NqWqlVjpUM5sNJcA0ZpwEGY1tpWMdc2FhrZOM6dkEiFbQF5O4CUA4Bh_Lx6d8x7iPPPBVPuJ58MjqMOOC-pZ5QpEFQU8M0_4H5eYii19YyxtnyrUgW6OEI7PWLvg5tz1KZMi5M3c0DnS3xbBIKqrlmf744CE-eUIrr-EP2k430PtF_d6_-61z-49yfEi_T1qaBlmNA-Ck92FeDtCdDJ6NFFHYxPDxwDoAJaWTh15FK5CjuMj539t4jfuBuwOA</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Valero, Antonio</creator><creator>de la Torre, Fernando</creator><creator>Castillo, José Antonio</creator><creator>Rivas, Pilar</creator><creator>del Cuvillo, Alfonso</creator><creator>Antépara, Ignacio</creator><creator>Borja, Javier</creator><creator>Donado, Esther</creator><creator>Molà, Oriol</creator><creator>Izquierdo, Iñaki</creator><general>Springer International Publishing</general><general>Adis International</general><general>Wolters Kluwer Health, Inc</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7T2</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7U2</scope></search><sort><creationdate>2009</creationdate><title>Safety of Rupatadine Administered Over a Period of 1 Year in the Treatment of Persistent Allergic Rhinitis</title><author>Valero, Antonio ; de la Torre, Fernando ; Castillo, José Antonio ; Rivas, Pilar ; del Cuvillo, Alfonso ; Antépara, Ignacio ; Borja, Javier ; Donado, Esther ; Molà, Oriol ; Izquierdo, Iñaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-d01195d6fe6b293251c9a1eb4c7dd792f75d1565f33f46e04d71e37b166b11c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Allergic diseases</topic><topic>Analysis</topic><topic>Antihistamines</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Clinical trial. Drug monitoring</topic><topic>Complications and side effects</topic><topic>Cyproheptadine - adverse effects</topic><topic>Cyproheptadine - analogs & derivatives</topic><topic>Cyproheptadine - therapeutic use</topic><topic>Development and progression</topic><topic>Dosage and administration</topic><topic>Drug Safety and Pharmacovigilance</topic><topic>Drug therapy</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>General pharmacology</topic><topic>Histamine H1 Antagonists - adverse effects</topic><topic>Histamine H1 Antagonists - therapeutic use</topic><topic>Humans</topic><topic>Immunopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medication Adherence - statistics & numerical data</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Non tumoral diseases</topic><topic>Original Research Article</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Patient compliance</topic><topic>Patient outcomes</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Respiratory and ent allergic diseases</topic><topic>Rhinitis</topic><topic>Rhinitis, Allergic, Perennial - drug therapy</topic><topic>Spain - epidemiology</topic><topic>Time Factors</topic><topic>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valero, Antonio</creatorcontrib><creatorcontrib>de la Torre, Fernando</creatorcontrib><creatorcontrib>Castillo, José Antonio</creatorcontrib><creatorcontrib>Rivas, Pilar</creatorcontrib><creatorcontrib>del Cuvillo, Alfonso</creatorcontrib><creatorcontrib>Antépara, Ignacio</creatorcontrib><creatorcontrib>Borja, Javier</creatorcontrib><creatorcontrib>Donado, Esther</creatorcontrib><creatorcontrib>Molà, Oriol</creatorcontrib><creatorcontrib>Izquierdo, Iñaki</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Safety Science and Risk</collection><jtitle>Drug safety</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valero, Antonio</au><au>de la Torre, Fernando</au><au>Castillo, José Antonio</au><au>Rivas, Pilar</au><au>del Cuvillo, Alfonso</au><au>Antépara, Ignacio</au><au>Borja, Javier</au><au>Donado, Esther</au><au>Molà, Oriol</au><au>Izquierdo, Iñaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety of Rupatadine Administered Over a Period of 1 Year in the Treatment of Persistent Allergic Rhinitis: A Multicentre Open-Label Study in Spain</atitle><jtitle>Drug safety</jtitle><stitle>Drug-Safety</stitle><addtitle>Drug Saf</addtitle><date>2009</date><risdate>2009</risdate><volume>32</volume><issue>1</issue><spage>33</spage><epage>42</epage><pages>33-42</pages><issn>0114-5916</issn><eissn>1179-1942</eissn><abstract>Background:
Rupatadine (Rupafin®), a novel antihistamine approved recently in Europe for the treatment of allergic rhinitis (AR) and chronic idiopathic urticaria in patients aged ≥12 years, has been shown to be highly efficacious, and as safe and well tolerated as other commonly employed antihistamines in the treatment of allergic disease. There are, however, few data on the long-term safety of these antihistamines derived in accordance with the clinical safety recommendations of the European Agency for the Evaluation of Medicinal Products (EMEA) and the International Conference on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use Guideline.
Objective:
To assess the safety and tolerability of treatment with rupatadine 10 mg/day for 12 months in subjects with persistent AR (PER).
Methods:
A multicentre, open-label, phase IV study in patients recruited from 33 centres in Spain, from September 2002 to November 2005. The study enrolled 324 male and female patients (aged 12–70 years) with a medical history of PER for at least 12 months and a documented positive skin-prick test to an appropriate allergen. On 4 of the 7 days prior to start of treatment, the patients were required to have a minimum total nasal symptom score (TNSS [for sneezing, rhinorrhoea, nasal obstruction/congestion and nasal itching]) of ≥5. Of the 324 eligible patients starting treatment, 120 needed to be treated for more than 6 months and were followed up until the end of 12 months. All patients received rupatadine 10 mg/day and were allowed to continue their normal concomitant medication for all conditions, other than rhinitis, for up to 6 or 12 months. Safety was assessed by means of adverse events (AEs) reported by patients or detected by investigators, scheduled centralized ECG with special attention to Bazzet corrected QT interval (QTcB) and standard laboratory investigations.
Results:
Assessment of treatment compliance rates indicated 90% and 83% of patients to be compliant during the 1–6 months and 1–12 months treatment periods, respectively, with compliance rates >80% being associated with the majority of the study population reporting at least one AE. Overall, 74.1% and 65.8% of the patients reported at least one AE during the 1–6 months and 1–12 months treatment periods, respectively, compared with 20.4% and 10.8% of patients reporting at least one treatment-related AE during these periods. Disorders of the nervous system and respiratory thoracic and media-stinal system, in particular headache, somnolence and catarrh, were the three most common AEs reported by >5% of the patients during both treatment periods. Detailed ECG assessments demonstrated no clinically relevant abnormal ECG findings, nor any QTcB increases >60 msec or QTcB values >470 msec for any patient at any time during treatment. Serious AEs were reported in seven patients, of whom six were considered as unlikely to be related to rupatadine treatment, whereas one involving increased blood enzyme levels was considered as possibly related to rupatadine treatment.
Conclusion:
This study confirmed the good long-term safety and tolerability of rupatadine at the therapeutic dose of 10 mg/day in patients with PER.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>19132803</pmid><doi>10.2165/00002018-200932010-00003</doi><tpages>10</tpages></addata></record> |
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source | Springer Nature |
subjects | Adolescent Adult Aged Allergic diseases Analysis Antihistamines Biological and medical sciences Child Clinical trial. Drug monitoring Complications and side effects Cyproheptadine - adverse effects Cyproheptadine - analogs & derivatives Cyproheptadine - therapeutic use Development and progression Dosage and administration Drug Safety and Pharmacovigilance Drug therapy Electrocardiography Female Follow-Up Studies General pharmacology Histamine H1 Antagonists - adverse effects Histamine H1 Antagonists - therapeutic use Humans Immunopathology Male Medical sciences Medication Adherence - statistics & numerical data Medicine Medicine & Public Health Middle Aged Non tumoral diseases Original Research Article Otorhinolaryngology. Stomatology Patient compliance Patient outcomes Pharmacology. Drug treatments Pharmacology/Toxicology Respiratory and ent allergic diseases Rhinitis Rhinitis, Allergic, Perennial - drug therapy Spain - epidemiology Time Factors Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology Young Adult |
title | Safety of Rupatadine Administered Over a Period of 1 Year in the Treatment of Persistent Allergic Rhinitis: A Multicentre Open-Label Study in Spain |
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