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  2. Excedrin (brand) - Wikipedia

    en.wikipedia.org/wiki/Excedrin_(brand)

    Excedrin Migraine continued the trend of marketing pain products for specific types of pain, becoming the first migraine headache medication available to consumers without a prescription, [9] even though it has identical active ingredients to the regular Excedrin Extra Strength product, 250 mg acetaminophen, 250 mg aspirin, and 65 mg caffeine ...

  3. Management of migraine - Wikipedia

    en.wikipedia.org/wiki/Management_of_migraine

    Rescue treatment involves acute symptomatic control with medication. [4] Recommendations for rescue therapy of migraine include: (1) migraine-specific agents such as triptans, CGRP antagonists, or ditans for patients with severe headaches or for headaches that respond poorly to analgesics, (2) non-oral (typically nasal or injection) route of administration for patients with vomiting, (3) avoid ...

  4. Triptan - Wikipedia

    en.wikipedia.org/wiki/Triptan

    The drugs of this class act as agonists for serotonin 5-HT 1B and 5-HT 1D receptors at blood vessels and nerve endings in the brain. The first clinically available triptan was sumatriptan, which has been marketed since 1991. Triptans have largely replaced ergotamines, an older class of medications used to relieve migraine and cluster headaches. [3]

  5. Excedrin Migraine vs. Extra Strength: Is There a Difference?

    www.aol.com/lifestyle/excedrin-migraine-vs-extra...

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  6. For the study, researchers looked at 137 controlled trials which tested oral drugs to treat migraine attacks. The trials involved a total of 89,445 patients who were given one of 17 drugs or a ...

  7. Rimegepant - Wikipedia

    en.wikipedia.org/wiki/Rimegepant

    Rimegepant, sold under the brand name Nurtec ODT among others, is a medication used for the acute treatment of migraine with or without aura in adults and the prophylactic/ preventive treatment of episodic migraine in adults. [8] [10] It is taken by mouth to dissolve on or under the tongue. [8] It works by blocking CGRP receptors. [11]

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