Frovatriptan (Frova) is a 5 HT-1 receptor agonist commonly called "Triptans". It causes intracranial vasoconstriction and is indicated for the treatment of patients with acute migraine attack. Frovatriptan has a very long half-life compared to other triptans (about five times that of other triptans) and hence, it may be indicated for the short-term prophylaxis of female patients with menstrual migraine.
Frovatriptan (Frova) Uses:
-
Migraines:
- Acute treatment of migraine with or without aura in adults
- Limitations of use: Do not use as prophylaxis. Use only in patients with confirmed diagnosis.
-
Off Label Use of Frovatriptan in Adults:
- Menstruation-associated migraines (short-term prevention)
Frovatriptan (Frova) Dose in Adults
Note: If no improvement seen consider alternate diagnosis. No safety data of treating more than four events each month.
Frovatriptan (Frova) Dose in the treatment of Migraine:
- Oral:
- Initial: 2.5 mg; if headache persistent repeat dose in 2 hours.
- The maximum recommended dose is 7.5 mg/day.
Use in Children:
Not indicated.
Frovatriptan (Frova) Pregnancy Category: C
- In animal reproduction studies, adverse events were reported.
- There are no data for humans. You can use other migraine medications during pregnancy.
Use Frovatriptan while breastfeeding
- Before starting treatment, analyze the risk-benefit ratio for both mother and baby.
Dose in Kidney Disease:
No dose adjustment is needed.
Frovatriptan (Frova) Dose in Liver disease:
-
Mild to moderate impairment:
- No dosage adjustment.
-
Severe impairment:
- No data are available.
Side Effects of Frovatriptan (Frova):
-
Cardiovascular:
- Flushing
- Hot Or Cold Flashes
- Chest Pain
- Palpitations
-
Central Nervous System:
- Dizziness
- Fatigue
- Headache
- Paresthesia
- Drowsiness
- Anxiety
- Dysesthesia
- Hypoesthesia
- Insomnia
- Pain
-
Dermatologic:
- Diaphoresis
-
Gastrointestinal:
- Xerostomia
- Nausea
- Dyspepsia
- Abdominal Pain
- Diarrhea
- Vomiting
-
Neuromuscular & Skeletal:
- Musculoskeletal Pain
-
Ophthalmic:
- Visual Disturbance
-
Otic:
- Tinnitus
-
Respiratory:
- Rhinitis
- Sinusitis
Contraindication to Frovatriptan (Frova):
- Ischemic coronary disease (eg angina pectoris; MI, documented silentischemia)
- Coronary artery vasospasm including Prinzmetal’s angina;
- Wolff-Parkinson White syndrome, arrhythmias and other cardiac accessory conduction pathway disorders
- History of stroke, transient Ischemia Attack, or hemiplegic migraine.
- Peripheral Vascular Disease;
- Ischemic bowel disease
- Hypertension uncontrolled
- Recent use within the last 24 hours of an ergotamine-containing or ergottype 5-HT-1 agonist (eg dihydroergotamine)
- hypersensitivity to any drug or component of the formula
Canadian labeling: Additional contraindications not in US labeling
- Cardiac arrhythmias (especially Tachycardia), valvular and congenital heart diseases, atherosclerotic diseases, and valvular heart disease are all possible.
- Management of ophthalmoplegic headaches
- Hepatic impairment severe
- There is not much evidence of triptan cross-reactivity.
- Cross-sensitivity is possible due to similarities in chemical structure or pharmacologic effects.
Warnings and precautions
-
Anaphylactoid and Anaphylactic reactions:
- Anaphylaxis, anaphylactoid and hypersensitivity reactions (including angioedema), may occur. If you are previously hypersensitive, it is contraindicated.
-
Cardiac events
- Administration of 5-HT-1 agonist has been associated with cardiac arrest, heart failure, transient ischemia and myocardial injury.
- Stop side effects developing
- Before continuing with treatment, patients who experience chest pain, pressure, tightness, or other symptoms that suggest angina should be examined for Prinzmetal's or CAD.
- If the patient experiences the same symptoms after treatment, ECG monitoring should be performed.
- Patients with vasospastic or ischemic CAD, Wolff-Parkinson White syndrome, or arrhythmias related to other cardiac accessory conduction pathways disorders are contraindicated.
-
Cerebrovascular events
- Contraindicated if you have a history of TIA/CVA.
- Five-HT-1 agonist administration has been linked to strokes and cerebral/subarachnoid hemorhage (some fatal).
-
High blood pressure
- Hypertension rarely with end-organ damage, or markedly elevated blood pressure.
- Contraindicated in conjunction with uncontrolled hypertension
-
Headaches
- If you take your medication for more than 10 days per month, withdrawal headaches can occur.
-
Vasospasm-related events
- Peripheral and gastrointestinal vascular infarction and infarction and Raynaud syndrome.
-
Visual effects
- There have been cases of partial and complete (reversible or irreversible) but no clear relationship.
-
Coronary artery disease
- Patients at high risk of developing CAD should be avoided (eg, hypertension and hypercholesterolemia; smoking obesity, diabetes, strong family history, men >40 years old, hypertension, smoking, or other factors that could increase the likelihood of developing CAD).
- Contraindicated for CAD and coronary artery vasospasm
- Before starting treatment, a cardiac evaluation is required. If you are using long-term treatment, follow up with periodic evaluation.
-
Hepatic impairment
- There are no data available. Please be careful.
Frovatriptan: Drug Interaction
|
Risk Factor C (Monitor therapy) |
|
|
Antiemetics (5HT3 Antagonists) |
May enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. |
|
Antipsychotic Agents |
Serotonin Modulators may enhance the adverse/toxic effect of Antipsychotic Agents. Specifically, serotonin modulators may enhance dopamine blockade, possibly increasing the risk for neuroleptic malignant syndrome. Antipsychotic Agents may enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. |
|
Droxidopa |
Serotonin 5-HT1D Receptor Agonists may enhance the hypertensive effect of Droxidopa. |
|
Metaxalone |
May enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. |
|
Methylphenidate |
May enhance the adverse/toxic effect of Serotonin Modulators. Specifically, the risk of serotonin syndrome or serotonin toxicity may be increased. |
|
Metoclopramide |
Serotonin Modulators may enhance the adverse/toxic effect of Metoclopramide. This may be manifest as symptoms consistent with serotonin syndrome or neuroleptic malignant syndrome. |
|
Opioid Agonists |
May enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. |
|
Serotonin Modulators |
May enhance the adverse/toxic effect of other Serotonin Modulators. The development of serotonin syndrome may occur. Exceptions: Nicergoline; Tedizolid. |
|
Tedizolid |
May enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. |
|
TraMADol |
Serotonin Modulators may enhance the adverse/toxic effect of TraMADol. The risk of seizures may be increased. TraMADol may enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. |
|
Risk Factor D (Consider therapy modification) |
|
|
Anti-Parkinson Agents (Monoamine Oxidase Inhibitor) |
May enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. Management: Monitor for signs and symptoms of serotonin syndrome/serotonin toxicity if selegiline, rasagiline, or safinamide is combined with a serotonin modulator. Use of transdermal selegiline with serotonin modulators is contraindicated. |
|
Linezolid |
May enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. Management: Due to a risk of serotonin syndrome/serotonin toxicity, discontinue serotonin modulators 2 weeks prior to the administration of linezolid. If urgent initiation of linezolid is needed, discontinue serotonin modulators immediately and monitor closely. |
|
Risk Factor X (Avoid combination) |
|
|
Dapoxetine |
May enhance the adverse/toxic effect of Serotonin Modulators. |
|
Ergot Derivatives |
May enhance the vasoconstricting effect of Serotonin 5-HT1D Receptor Agonists. Serotonin 5-HT1D Receptor Agonists may enhance the vasoconstricting effect of Ergot Derivatives. Exceptions: Nicergoline. |
|
Methylene Blue |
May enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. |
|
SUMAtriptan |
Serotonin 5-HT1D Receptor Agonists may enhance the adverse/toxic effect of SUMAtriptan. |
Monitoring parameters:
- Severity of headache severity
- bloodpressure
- signs/symptoms of angina. Periodic cardiac function assessment inwin patients with long duration of therapy and multiple cardiovascular risk factors.
- signs/symptoms of serotonin syndrome and hypersensitivity reactions.
How to administer Frovatriptan (Frova)?
- Take when symptoms appear. Wash down with lots of fluids
Mechanism of action of Frovatriptan (Frova):
- Selective serotonin antagonist (5-HT-1B or 5-HT-1D receptors), in the cranial arteries.
- Reduces migraines due to migrane headaches by increasing blood flow and decreasing inflammation.
Protein binding:
- ~15%
Metabolism:
- Primarily hepatic via CYP1A2
Bioavailability:
- Male: ~20%;
- Female: ~30%
Half-life elimination:
- ~26 hours
Time to peak:
- 2-4 hours
Excretion:
- Feces (62%);
- Urine (32%)
International Brand Names of Frovatriptan:
- Frova
- APO-Frovatriptan
- TEVA-Frovatriptan
- Allegro
- Auradol
- Eumitan
- Forvey
- Fromen
- Fromena
- Fromirex
- Frovatex
- Frovex
- Menamig
- Menatriptan
- Migard
- Miguard
- Relieva
- Tigreat
Frovatriptan Brands Names in Pakistan:
No Brands Available in Pakistan.