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Global: Bridge EU Pregnancy Report Form FOR ROCHE USE ONLY Roche Received Date (ddMMMyyyy):Local No: ProspectiveReport Type: 1.AER No: RetrospectiveNote: If available please provide reporters occupation.
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Global Erivedge EU pregnancy refers to the reporting requirements for pregnant women who have been exposed to the drug Erivedge in the European Union.
Healthcare providers, including doctors and pharmacists, are required to file global Erivedge EU pregnancy reports.
Global Erivedge EU pregnancy reports can be filled out online through the designated reporting system or by contacting the relevant regulatory authorities.
The purpose of global Erivedge EU pregnancy reporting is to monitor the safety of the drug Erivedge in pregnant women and their unborn babies.
Information such as the patient's demographics, details of exposure to Erivedge, pregnancy outcomes, and any adverse events must be reported on global Erivedge EU pregnancy reports.
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