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Soon, in 1994, ICOS received a patent for compound IC351 (structurally unlike sildenafil and vardenafil), and Phase 1 clinical trials began in 1995. In 1997, the Phase 2 clinical studies were initiated for males experiencing ED, then progressed to the Phase 3 trials that supported the drug’s FDA approval. Two years later, Lilly ICOS, LLC, filed a new drug application with the FDA for compound IC351 (under the tadalafil generic name, and the Cialis brand name).

If you experience any side effects, whether they are listed above or in the patient information leaflet, speak to your doctor or call 111 for advice. For more information regarding the safety of this medication, we encourage you to read the patient information leaflet enclosed within the packaging. You can become aware of the side effects by&nbsp