WHO Pharmaceuticals Newsletter 2002, No. 03
(2002; 22 pages) View the PDF document
Table of Contents
Close this folderREGULATORY MATTERS
View the documentARISTOLOCHIC ACID - Warnings on more products containing Aristolochic acid
View the documentARTHRIN, OSPORO, POENA AND OTHERS - Presence of undeclared prescription drugs poses health threat
View the documentASPIRIN - Restrictions on use in children extended to teenagers
View the documentBACLOFEN - Life threatening sequelae and/or death with abrupt withdrawal of intrathecal injections
View the documentBEJAI BOWYANTAN - Risk of toxicity in children due to presence of Borneol
View the documentCELECOXIB - CLASS findings added to product label
View the documentEPOETIN-ALFA - Important safety update
View the documentGLITAZONES - strengthens labelling for cardiovascular risks
View the documentHORMONE REPLACEMENT THERAPY (HRT) - Product information updated
View the documentIRINOTECAN - Labelling updated
View the documentKAVA-KAVA - More withdrawals due to hepatotoxic risks
View the documentMELOXICAM - Additional information in package insert
View the documentMISOPROSTOL - Major labelling changes
View the documentNIMESULIDE - Temporary suspension pending further evaluation
View the documentOLANZAPINE - Risk of hyperglycaemia
View the documentPOOLED PLASMA (HUMAN) SOLVENT DETERGENT TREATED - Boxed warning to indicate new contraindication
View the documentPROPOFOL - Contraindication section modified
View the documentROFECOXIB - Reports of gastrointestinal/cardio vascular toxicity; labelling updated
View the documentSIROLIMUS - Correction to drug safety information
View the documentSLIM 10 - Withdrawn due to presence of adulterants
View the documentTAMOXIFEN - Boxed warning added to product label
View the documentTETRABAMATE - Withdrawal due to reports of hepatotoxicity
View the documentVALPROATE - Labelling strengthened
View the documentZONISAMIDE - Prescribing information updated
Open this folder and view contentsSAFETY OF MEDICINES
Open this folder and view contentsDRUGS OF CURRENT INTEREST
Open this folder and view contentsFEATURE
View the documentEVENTS & ANNOUNCEMENTS
 

MELOXICAM - Additional information in package insert

Sultanate of Oman. The Directorate General of Pharmaceutical Affairs and Drug Control (DGPA&DC) of Oman has approved the addition of the following information in the package insert of meloxicam (Moven) capsules:

Drug Interaction: Meloxicam is not recommended with concomitant aspirin therapy due to the possibility of an increase in gastrointestinal ulceration or other complications.

Side Effects: Concomitant use of meloxicam, 15 mg once daily, and lithium doses ranging from 804 to 1072 mg twice daily are known to result in an increase in the mean pre-dose lithium concentration and the area under the curve by 21% when compared to subjects receiving lithium alone. This results from an inhibition of renal prostaglandin synthesis by meloxicam.

Reference:

Pharmaceutical Newsletter of the Ministry of Health, Sultanate of Oman, vol. 10 (1), 2002.

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Last updated: May 3, 2013