What's new
Newsletters "UptoDate" of BASG/AGES MEA are published monthly and contain the latest articles from the last month (link to subscription page).
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28/10/2016
other persons and other administrators for the company and can also change data of persons, (in)activate or delete persons in the user and role management console. Furthermore the administrator has the
Referenced at:
28/10/2016
other persons and other administrators for the company and can also change data of persons, (in)activate or delete persons in the user and role management console. Furthermore the administrator has the
Referenced at:
Recall
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Medicines
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18/10/2016
Gedeon Richter Plc has informed their supplied customers by letter dated 12/10/2016 that above mentioned batches of "Lisvy 60 microgram/24 hours + 13 microgram/24 hours Transdermal Patch" are recalled. Stability data for these batches indicated a…
Safety warnings
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messages in brief
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17/10/2016
Several cases of accidental overdose associated with Levetiracetam - Oral Solution have been reported throughout Europe. The majority of cases involved children between 6 months and 11 years of age. Many of these unintentional medication errors…
Recall
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Medicines
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14/10/2016
CSL Behring as distributor of the product Helixate NexGen has, in coordination with the marketing authorization holder Bayer Pharma AG, informed its supplied customers in a letter dated October 11, 2016, that the above mentioned batches of Helixate…
Safety warnings
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Blood & Tissue
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20/09/2016
The Federal Office for Public Health Safety has been informed by the Greek authority that another confirmed locally acquired malaria case has been recorded in Greece. No travel activity of the infected person is known.
Safety warnings
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Blood & Tissue
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25/08/2016
The Federal Office for Public Health Safety has been informed by the Greek authority that four confirmed locally acquired malaria cases have been recorded in Greece (two in the western Peloponnese and two in central Macedonia).
Recall
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Veterinary Medicines
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02/08/2016
The distribution company "Chevita Tierarzneimittel Ges.m.b.H." has informed its supplied customers with 05.07.2016 that in the course of stability tests a reduced content of active ingredient was found and therefore the affected packages of this drug…
Recall
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Medicines
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15/07/2016
The marketing authorization holder has informed its supplied customers in a letter dated 14.07.2016 that the title of the leaflet is incorrect. The active strength is listed as 5 mg instead of 10 mg and therefore the affected batches of "Amlodipine…
Recall
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Medicines
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21/04/2016
The marketing authorization holder informed its supplied customers in a letter dated 19.04.2016 that an error in the filling process was detected at the manufacturer. The error results in a few vials possibly containing a too high concentration. The…