Pharmacoeconomic review report. AbobotulinumtoxinA (Dysport therapeutic) (Ipsen Biopharmaceuticals Canada, Inc.).

AbobotulinumtoxinA (aboBoNTA, Dysport Therapeutic) is a botulinum neurotoxin subtype indicated to reduce the subjective symptoms and objective signs of cervical dystonia (CD, spasmodic torticollis) in adults, and is available in single-use vials of 300 U and 500 U at submitted prices of $428.40 and...

Full description

Saved in:
Bibliographic Details
Online Access: http://www.ncbi.nlm.nih.gov/books/NBK535069/
Full text
Format: Electronic eBook
Language:English
Published: Ottawa (ON) : Canadian Agency for Drugs and Technologies in Health, 2017
Series:Common drug review clinical review report.
Subjects:

MARC

LEADER 00000cam a2200000 i 4500
001 p2436907
005 20240212122442.0
006 m o d
007 cr cn ||||||||
008 190102s2017 onca ob 000 0 eng
035 |a (DNLM)BKSHLF:NBK535069 
035 |9 101740873 
035 |a 1740873 
040 |a DNLM  |b eng  |e rda  |c DNLM  |d UtOrBLW 
041 0 9 |a eng 
042 |a pcc 
043 |a n-cn--- 
044 |9 Canada 
060 0 0 |a WE 708 
245 0 0 |a Pharmacoeconomic review report.  |p AbobotulinumtoxinA (Dysport therapeutic) (Ipsen Biopharmaceuticals Canada, Inc.). 
246 1 |a Pharmacoeconomic review report for Dysport therapeutic 
246 1 |a AbobotulinumtoxinA (Dysport therapeutic) (Ipsen Biopharmaceuticals Canada, Inc.) 
264 1 |a Ottawa (ON) :  |b Canadian Agency for Drugs and Technologies in Health,  |c August 2017. 
300 |a 1 online resource (1 PDF file (16 pages)) :  |b illustrations. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a CADTH common drug review 
500 |a "Version: Final." 
504 |a Includes bibliographical references. 
520 3 |a AbobotulinumtoxinA (aboBoNTA, Dysport Therapeutic) is a botulinum neurotoxin subtype indicated to reduce the subjective symptoms and objective signs of cervical dystonia (CD, spasmodic torticollis) in adults, and is available in single-use vials of 300 U and 500 U at submitted prices of $428.40 and $714.00, respectively. The recommended initial dose of aboBoNTA is 500 U intramuscularly as a divided dose among affected muscles in patients with and without a prior history of treatment with botulinum toxin. Re-treatment of 250 U to 1,000 U divided among affected muscles is recommended when the effect of a previous injection has diminished, but no sooner than 12 weeks after the previous injection. The manufacturer is requesting that aboBoNTA be reimbursed in line with its indication. 
536 |a Funding: CADTH receives funding from Canada's federal, provincial, and territorial governments, with the exception of Quebec. 
588 |a Description based on online resource; title from PDF title page (viewed February 21, 2019). 
650 1 2 |a Torticollis  |x drug therapy.  |0 D014103Q000188 
650 2 2 |a Botulinum Toxins, Type A  |x therapeutic use.  |0 D019274Q000627 
650 2 2 |a Cost-Benefit Analysis.  |0 D003362 
651 2 |a Canada.  |0 D002170 
710 2 |a Canadian Agency for Drugs and Technologies in Health,  |e issuing body.  |0 n 2007182676 
830 0 |a Common drug review clinical review report.  |0 n 2014186107 
856 4 0 |u http://www.ncbi.nlm.nih.gov/books/NBK535069/  |t 0 
951 |a 2436907 
992 |p P2  |e EF  |a 20190102 
993 |a KXP  |b 20190212 
995 |a AUTH  |b 20190221  |c REV  |d 20190227 
998 |a BKSHLF  |b 20190102 
998 |a FER  |b 20190102 
999 |a AUTH 
999 f f |i 9f2435fa-d6ca-5998-b976-2b1300736081  |s d1ae0ace-8aa1-5cec-bed4-7b274a2bbc63  |t 0 
952 f f |a Massachusetts College of Pharmacy and Health Sciences  |b Online  |c Online  |d E-Collections  |t 0  |e NCBI  |h Other scheme 
856 4 0 |t 0  |u https://www.ncbi.nlm.nih.gov/books/NBK535069/  |y Full text