FROVA
Pronunciation: froe-va-TRIP-tan (FROE-va)

What it is5-HT1B/1D agonist with the longest half-life of the triptans; acute migraine.
Why this oneThe long duration suits menstrual migraine, where it is used for short-term prevention.
What limits itSlow onset, so it is wrong for a fast attack. Coronary vasospasm.
Read the full label on DailyMed ↗
| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Acute migraine | Adults | 2.5 mg PRN | 2.5 mg PRN | 7.5 mg (3 tablets)/24h |
Renal Undefined
Hepatic Undefined
Second dose ≥2 h after first; max 3 tablets/24h; no evidence a 2nd dose helps initial non-responders
Available strengths
Pregnancy No adequate human data; developmental toxicity in animals at higher-than-clinical doses
Lactation No human data; present in rat milk
| Strength | #/mo | generic $/unit | CostPlus | |
|---|---|---|---|---|
| 2.5 mg | tab | per unit | $2.72/ea | offered |
Generic entry2014
NO BOXED WARNINGS
Principal riskSlow onset; coronary vasospasm
Legacy pregnancy categoryUnknown / historical label unavailable
Defining liabilityAgent-specific vascular, serotonergic or hepatic risks; acute overdose is usually limited outside ergot or cardiovascular agents.
This drug is routinely called serotonergic. By Gillman’s human-effect criteria it does not raise serotonin in the synapse.
Triptan receptor agonism is not a mechanistic serotonin-toxicity interaction with SRIs.
Gillman’s four human testsA measurable SERT affinity that fails all four is not clinical serotonicity.
Non-elevating action5-HT1B/1D agonist
Evidence confidenceHigh
Background: what serotonicity is · what is and is not an SRI · what counts as a relevant MAOI.