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Notice

HUMANS VARY IN THEIR BIOLOGICAL REACTIONS TO MEDICINAL PRODUCTS. THIS IS WHY NOT ALL ADVERSE REACTIONS (SIDE EFFECTS) ASSOCIATED WITH THE USE OF MEDICINAL PRODUCTS CAN BE DETECTED DURING CLINICAL DEVELOPMENT, NOT EVEN BY THE MOST COMPREHENSIVE CLINICAL TRIALS. CAPTURING AS MANY OF THESE ADVERSE REACTIONS, HOWEVER RARE THEY MAY BE IN ABSOLUTE TERMS, FROM WORLDWIDE SOURCES IS OF PARAMOUNT IMPORTANCE FOR CONTINUED PATIENT AND DRUG SAFETY (PHARMACOVIGILANCE).

FOR BAYER AS A GLOBAL PHARMACEUTICAL COMPANY, PHARMACOVIGILANCE TAKES CENTER STAGE, BEYOND MORE COMPLIANCE WITH WORLDWIDE REGULATIONS. TO ENABLE BAYER TO PROVIDE UP-TO DATE SAFETY INFORMATION ON BAYER PRODUCTS, YOUR SUPPORT IS PIVOTAL, WHETHER YOU ARE A CUSTOMER, PATIENT OR HEALTHCARE PROFESSIONAL.

IF YOU WANT TO REPORT A SIDE EFFECT OR QUALITY COMPLAINT, PLEASE CONTACT YOUR HEALTHCARE PROFESSIONAL (E.G. PHYSICIAN OR PHARMACIST) OR YOUR LOCAL HEALTH AUTHORITY.

REPORTS CAN ALSO BE MADE ON OUR

SIDE EFFECT REPORTING WEBSITE.

For further details, please contact:

Bayer Limited Egypt LLC
Mivida – Business Park 3
B1 Building – 2nd. Floor

P.O.Box: 133
New Cairo - Cairo, Egypt

Phone: +202 2598 0666
Web: https://middleeast.bayer.com

* For Medical Inquiries, send to: bme.ch-medinfo@bayer.com
** For Safety Reporting: www.safetrack-public.bayer.com or pv.me@bayer.com
*** Information sent to the above contact details is subject to Bayer Privacy Statement (https://me-privacy.baywsf.com/) and/or Bayer Privacy Statement for Pharmacovigilance Data (https://www.bayer.com/en/privacy-statement-pv) and might be transferred outside your country, including but not limited to, transfer outside the United Arab Emirates & Saudi Arabia