Declaration of adverse events
To submit to us any adverse event likely to be due to the taking and/or prescription and/or delivery of our products, simply complete the adverse event reporting form by clicking here.
You can also report to the CNPM (National Center for Pharmacovigilance and Materiovigilance) on the website www.cnpm.org.dz, any adverse event, adverse effect, incident or risk of incident related to a health product.
By reporting adverse effects, you contribute to improving knowledge of the tolerance profile of products.
To find out more about PHARMACOVIGILANCE, consult the 1st issue of our online booklet:
Email : pharmacovigilance@ldmgroupe.com
Phone : (24h/24, 7d/7) : (+213) 982 30 45 45
(+213) 30 30 71 88 / (+213) 30 30 73 63
Mobile (24h/24, 7d/7) : (+213) 561 70 11 62
OR
Complete this adverse event reporting form by clicking here.
LDM takes the protection of personal data very seriously. We adhere to applicable national and EU data protection regulations and will collect and process any personal data you provide in accordance with our Pharmacovigilance Data Privacy Policy.
CNPM, Sis Route Petit Staoueli (NIPA) Dely Ibrahim Alger,
Tel / Fax : +213 23 36 75 02 / +213 23 36 75 27 / +213 23 36 75 29
Email : cnpm@cnpm.org.dz
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