Controversy Over Human Drugs for Pets; Lin Ching-yi Emphasizes Respecting Vets and Solving Problems Together
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As the new regulation on using human drugs for pets approaches in July, concerns over veterinary drug shortages have arisen. The Ministry of Health and Welfare stated it aims to track drug flows to ensure supply resilience while respecting veterinary needs.
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Frequently Asked Questions
- Q: What regulations will officially take effect in July after a two-year buffer period?
- A: The Regulations on the Use and Management of Human Medicines for Dogs, Cats, and Non-Economic Animals will take effect.
- Q: How many human drugs on the positive list have been registered by pharmaceutical companies so far?
- A: Only 216 out of 701 items on the positive list have been registered, which is less than 30 percent.
- Q: Why does the workaround for pet medication fail to account for nighttime and emergency needs?
- A: It requires pet owners to take veterinary prescriptions to pharmacies and then bring the drugs back to veterinarians.
- Q: What are the respective responsibilities of APHIA and the FDA regarding animal and human drugs?
- A: APHIA is the competent authority for veterinary drugs, while the FDA manages pharmaceutical factories and drug quality.
- Q: What did the Ministry of Health and Welfare emphasize in its six-point statement?
- A: The Ministry emphasized its hope to promote institutional development through cross-departmental cooperation.