№ files_lp_4_process_2_69384
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This document contains detailed information on the composition of bOPV vaccine, including active and other ingredients, and their respective concentrations.
Year:
N/A
Region / City:
N/A
Topic:
Vaccine composition
Document Type:
Supplementary Table
Author:
N/A
Target Audience:
N/A
Period of Validity:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2025
Region / city:
[insert local health board name]
Subject:
Pharmaceutical Service, Public Health
Document type:
Patient Group Direction (PGD)
Organ / institution:
Welsh Medicines Advice Service, NHS Wales
Author:
Dianne Burnett, National Lead Pharmacist, Medicines Advice
Target audience:
Pharmacists, Healthcare professionals
Validity period:
01 April 2025 – 31 March 2028
Approval date:
11 February 2025
Amendment date:
06 January 2025
Year:
2024-2025
Region / City:
Washington State
Topic:
Medical authorization form
Document Type:
Medical Authorization
Organization:
Washington State School for the Blind
Author:
Licensed Health Professional
Target Audience:
Parents/Guardians, School Staff
Effective Period:
07/01/2024 - 08/31/2025
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2019
Region / city:
Australia
Topic:
Medical device, eye care
Document type:
Public Summary Document
Organ / institution:
Therapeutic Goods Administration (TGA), Pharmaceutical Benefits Advisory Committee (PBAC)
Author:
Allergan Australia Pty Ltd
Target audience:
Healthcare professionals, medical practitioners
Period of validity:
Not specified
Approval date:
13 March 2019
Date of amendments:
Not specified
Note:
Date
Follow the Six Rights of Medication Administration:
Right student, Right medication, Right dose, Right time, Right route and Right documentation. Know which eye is to be treated. Initials may be used to specify the eye that requires treatment, O.D. = right eye; O.S. = left eye; O.U. = both eyes.
Topic:
Medication administration
Document Type:
Training checklist
Organization:
School
Author:
Not specified
Target Audience:
Staff administering medication
Period of validity:
School year
Year:
2019
Region / city:
Australia
Subject:
Medical Device Registration
Document Type:
Medical Application
Organization:
Seqirus (Australia) Pty Ltd
Author:
Seqirus
Target Audience:
Medical practitioners, optometrists, and healthcare professionals
Period of validity:
Not specified
Approval Date:
July 2019
Modification Date:
Not specified
Medicine:
Ciclosporin 1 mg/mL (0.1%) eye drops
Brand name:
Ikervis®
Sponsor:
Seqirus (Australia) Pty Ltd
Regulatory authority:
Therapeutic Goods Administration (TGA)
Registration date:
11 December 2020
Program:
Pharmaceutical Benefits Scheme (PBS)
Restriction type:
Authority Required (Streamlined)
Schedule category:
GENERAL – General Schedule (Code GE)
Indication:
Treatment of severe keratitis in adult patients with dry eye disease not improved despite tear substitutes
Population:
Patients aged 18 years or older with severe keratitis and dry eye disease
Comparators:
Best supportive care including preservative free artificial tears
Clinical criteria (initiation):
Corneal fluorescein staining grade 4 (modified Oxford scale or equivalent) and OSDI ≥ 23; failure of optimised preservative free tear substitutes
Clinical criteria (continuation):
Demonstrated adequate response at 6 months
Definition of adequate response:
Improvement in CFS ≥ 3 grades and ≥ 30% improvement in OSDI from baseline
Prescriber restrictions:
Ophthalmologist or optometrist
Economic basis:
Cost-utility analysis versus best supportive care
Proposed treatment phases:
Initiation; continuation; continuation after assessment of response
Year:
2026
Region / City:
N/A
Topic:
Veterinary medicine, Antibiotics
Document Type:
Instruction Manual
Author:
N/A
Target Audience:
Pet owners, Veterinarians
Expiration Period:
14 days after mixing
Approval Date:
N/A
Date of Changes:
N/A
Date:
April 23, 2020
Artist:
Goody Grace
Song Title:
If I Want To
Genre:
Alternative, Pop-punk
Label:
Atlantic Records
Featured Artist:
BLINK 182
Producer(s):
Goody Grace, Jake Torrey, afterhrs
Songwriter(s):
Goody Grace, Jake Torrey
Lyric Video:
Yes
Streaming Platforms:
All DSPs and streaming services
Playlist:
"I’ll Get High If I Want To" (SPIN)
Press Contact:
Jessica Nall / [email protected], Jason Davis / [email protected], Megan Rasmussen (Tour) / [email protected]
Description:
Press release for the new single “If I Want To” by Goody Grace, a 4/20-friendly anthem that interpolates Lesley Gore’s “It’s My Party” with a modern twist, following the success of “Scumbag” featuring BLINK 182.
Note:
Year
Context description:
A submission for the inclusion of perfluorohexyloctane eye drops in the PBS list for severe dry eye syndrome treatment in patients sensitive to preservatives.
Year:
2023
Region / city:
Gulf
Topic:
Stock Markets, Oil Prices
Document Type:
Financial Report
Organization / Institution:
Reuters
Author:
Reuters
Target Audience:
Investors, Financial Analysts
Period of validity:
2023
Approval Date:
2023
Date of Changes:
N/A
Year:
2006
Region / City:
Australia
Topic:
Medication management, disability services
Document Type:
Legal / Regulatory
Organization:
Disability Services
Author:
Not specified
Target Audience:
Healthcare providers, professionals in disability services
Effective Period:
Ongoing
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2023
Region / City:
Australia
Subject:
Chronic migraine, medicinal product submission
Document type:
Submission for PBS listing
Organization:
Novartis Pharmaceuticals Australia Pty. Limited
Author:
Not specified
Target audience:
Health professionals, pharmaceutical regulatory bodies
Period of validity:
Not specified
Date of approval:
2 July 2018
Date of amendments:
November 2023
Year:
2024
Regulatory authority:
Therapeutic Goods Administration (TGA)
Medicine:
MACITENTAN 10 mg with TADALAFIL 40 mg (Opsynvi®)
Indication:
Pulmonary arterial hypertension (PAH), WHO Group 1, functional class II and III
Therapy type:
Dual or triple combination therapy
Dosage form:
Tablet, fixed dose combination (FDC)
Prescriber type:
Medical practitioners
Restriction type:
Authority Required (Written, Complex Authority Required)
Clinical criteria:
Treatment as dual therapy (MAC+TAD) or triple therapy with prostanoid
Population:
Adult patients with stable PAH on separate doses of macitentan and tadalafil
Previous considerations:
PBAC recommendations for macitentan and tadalafil since 2011–2014
Approval date:
16 September 2024
Source documents:
TGA registration, PBAC meeting minutes, ACM minutes August 2024, FDA, EMA, CDA references
Note:
Year
Subject:
High Dose Antipsychotic Monitoring
Document Type:
Medical Form
Institution:
Oxford Health
Target Audience:
Healthcare professionals
Year:
2024
Region / city:
United Kingdom
Subject:
Radiological Protection, Transport of Radioactive Materials
Document Type:
Technical Assessment Guide
Organization:
Office for Nuclear Regulation (ONR)
Author:
Inspector - Nuclear Safety
Target Audience:
ONR safety inspectors
Validity Period:
October 2024 - October 2029
Approval Date:
October 2024
Revision Date:
Not applicable
Document Reference:
NS-TAST-GD-100
Record Reference:
2020/281169
Issue:
2.1
Purpose:
Guidance for assessing shielding designs and dose rates of transport packages for radioactive materials.
Scope:
Focuses on shielding and dose rate assessments in accordance with IAEA regulations for transport safety.
Related Legislation:
IAEA SSR-6 (2018), UK regulations for radioactive materials transport
Note:
Contextual Description
Year:
Not specified
Region / City:
Not specified
Topic:
Infliximab dose escalation in Crohn’s disease treatment
Document type:
Medical request letter
Institution / Organization:
Not specified
Author:
Not specified
Target audience:
Insurance company
Period of validity:
Not specified
Approval date:
Not specified
Date of modifications:
Not specified
Note:
Year
Topic:
Lung disease, steroid treatment
Document type:
Information sheet
Organization / institution:
Sheffield Teaching Hospitals NHS Foundation Trust
Author:
Respiratory and endocrinology teams
Target audience:
People with lung disease on high dose inhaled steroids
Year:
2023
Region / city:
Canberra, Australia
Topic:
Obstetrics, Pre-eclampsia, Pregnancy Care
Document type:
Guideline
Organization / institution:
Canberra Health Services
Author:
Society of Obstetric Medicine Australia and New Zealand (SOMANZ)
Target audience:
Medical Officers, Registered Nurses, Registered Midwives, Students, Pharmacists
Period of validity:
Not specified
Approval date:
2023
Date of amendments:
Not specified
Year:
2022
Region / City:
Australia
Subject:
Pharmacology, Pharmaceutical Benefits Scheme (PBS)
Document Type:
Submission
Organization / Institution:
Sanofi-Aventis Australia Pty Ltd
Author:
Not specified
Target Audience:
Medical practitioners, healthcare professionals
Period of validity:
Not specified
Approval Date:
3 June 2022
Date of Changes:
Not specified
Contextual Description:
A regulatory submission detailing the request for listing of dupilumab in new forms for treating severe atopic dermatitis and uncontrolled severe asthma in pediatric patients under the PBS.
Note:
Year
Background:
The submission requested a General Schedule Authority Required (Telephone/Online) listing of a new form of adrenaline (epinephrine) acid tartrate 150 micrograms/0.15 mL autoinjector (AI) (Jext® Junior (Jr)) and 300 micrograms/0.3 mL AI (Jext®) under the same circumstances as the currently listed adrenaline (epinephrine) 150 microgram/0.3 mL AI (EpiPen® Jr and Anapen® Jr 150) and 300 microgram/0.3 mL AI (EpiPen® and Anapen® 300).