Šalis: Kanada
kalba: anglų
Šaltinis: Health Canada
IPRATROPIUM BROMIDE
PHARMASCIENCE INC
R03BB01
IPRATROPIUM BROMIDE
21MCG
SOLUTION
IPRATROPIUM BROMIDE 21MCG
NASAL
30ML
Prescription
ANTIMUSCARINICS ANTISPASMODICS
Active ingredient group (AIG) number: 0115643002; AHFS:
APPROVED
1999-02-12
_ _ _pms-IPRATROPIUM Product Monograph _ _Page 1 of 26_ PRODUCT MONOGRAPH PR PMS-IPRATROPIUM (Ipratropium Bromide Nasal Spray) 0.03% w/v (21 μg/metered spray) TOPICAL ANTICHOLINERGIC FOR NASAL ADMINISTRATION PHARMASCIENCE INC. 6111 Royalmount Ave., Suite 100 Montreal, Quebec H4P 2T4 Date of Revision: October 26, 2012 Submission Control No: 157146 _ _ _pms-IPRATROPIUM Product Monograph _ _Page 2 of 26_ TABLE OF CONTENTS PART I: HEALTH PROFESSIONAL INFORMATION .........................................................3 SUMMARY PRODUCT INFORMATION ........................................................................3 INDICATIONS AND CLINICAL USE ..............................................................................3 CONTRAINDICATIONS ...................................................................................................3 WARNINGS AND PRECAUTIONS ..................................................................................3 ADVERSE REACTIONS ....................................................................................................4 DRUG INTERACTIONS ....................................................................................................8 DOSAGE AND ADMINISTRATION ................................................................................9 OVERDOSAGE ..................................................................................................................9 ACTION AND CLINICAL PHARMACOLOGY ............................................................10 STORAGE AND STABILITY ..........................................................................................14 DOSAGE FORMS, COMPOSITION AND PACKAGING .............................................14 PART II: SCIENTIFIC INFORMATION ...............................................................................15 PHARMACEUTICAL INFORMATION ..........................................................................15 CLINICAL TRIALS .............................................................................. Perskaitykite visą dokumentą