Guest
Guest
May 26, 2025
1:46 AM
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Tadalista Professional (a sublingual tadalafil tablet), you can contact the appropriate drug safety authority in your country. Here's how to report: ???? If You're in the United States Since Tadalista Professional is not FDA-approved (it is a foreign-manufactured generic), you should still report adverse effects To the FDA: Online: FDA MedWatch Reporting Phone: 1-800-FDA-1088 Mail or Fax: Use the MedWatch 3500 form (available on the FDA website) ???? If You're in India Tadalista is manufactured in India (usually by Fortune Healthcare), and side effects should be reported t PvPI (Pharmacovigilance Programme of India) Online: PvPI ADR Reporting Form Phone: 1800-180-3024 (toll-free) Email: Other Countries For other countries, report to your national regulatory body: UK: MHRA Yellow Card Scheme Canada: Health Canada MedEffect Australia: Therapeutic Goods Administration (TGA) ?? What to Include in Your Report Drug name: Tadalista Professional Dosage taken (e.g., 20 mg) Symptoms experienced When symptoms started Any other medications or conditions Where you purchased it (if applicable)
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