FDA approves onabotulinumtoxinA to prevent chronic migraine
FDA has approved onabotulinumtoxinA (Botox, Allergan Inc.) injection to prevent headaches in adult patients with chronic migraine.
FDA has approved onabotulinumtoxinA (Botox, Allergan Inc.) injection to prevent headaches in adult patients with chronic migraine. OnabotulinumtoxinA is injected about every 12 weeks at multiple sites around the head and neck to try to dull future headache symptoms.
Irvine, Calif.-based Allergan provided FDA substantial evidence of safety and effectiveness to support the new indication of prophylaxis of headaches in patients with chronic migraine, an agency spokesperson told Formulary.
Botox has not been shown to work for the treatment of migraine headaches that occur 14 days or less per month or for other forms of headache.
FDA Clears Phase 2 Trial of Cannabis in PTSD
November 20th 2024After a three-year negotiation, the FDA has dropped its objection to allowing patients to self-titrate dosing of smoked cannabis. But regulators want to see additional information about the device that will be used for inhalation.
Read More
