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Description
Follicle Pharma A phase 1 trial of FOL100 began in October 2022 and is expected to continue throughout the year
The FDA has not issued formal reclassification guidance
We believe that informed patients make empowered decisions
(2021) 100:e26707
To report SUSPECTED ADVERSE EVENTS, contact Actavis at 1-800-272-5525 or FDA at 1-800-FDA-1088 or for voluntary reporting of adverse reactions
