Iprazochrome is an
antimigraine agent used for prophylaxis of the attacks. It is also indicated for
diabetic retinopathy (both treatment and prevention in people with type-2 diabetes).
Chemically, it is a derivative of
adrenochrome, which is a product of
adrenaline oxidation. And it is a derivative of
carbazochrome as well.
This drug decreases the permeability and fragility of blood vessels, which reduces the number of migraine days and attenuates the symptoms associated with this condition, but it does not eliminate them altogether.
In animal models, iprazochrome was shown not to decrease the
spreading depression velocity, which is a feature of other antimigraine agents and is thought to be one of the essential causes of classical migraines.[2]
Dose
For migraines, 1-3 tabletes (each tablet contains 2.5 mg of iprazochrome) are taken three times a day. An abortive medication is recommended in the first weeks of treatment.
For diabetic retinopaty, 2 tablets are taken three times a day. If the initial treatment was successful, it can be reduced to 1 tablet three times a day.
The effect of this medication is usually seen after a month. It's achieves its full efficacy after 3 months of treatment.
Side effects
It can work as an anorectic and can cause skin allergic reactions after discontinuing.
This drug was also shown to induce pain in patients with atypical facial pain.[1]
Pharmacokinetics
Absorption
After taking the drug on empty stomach, it is rapidly absorbed. Peak serum concentration (
Cmax) is achieved after 1 hour, but its effect on blood vessels is seen only after 3 hours.
Elimination
The
half-life of iprazochrome is 2.2 hours. It is metabolised renally and 20% is eliminated in an unchanged form.
There are two known metabolites of iprazochrome: an
indole derivative (detected in urine) and a 6-hydroxy derivative (detected in feces).
References
^
abHampf G (1989). "Effect of serotonin antagonists on patients with atypical facial pain". Journal of Craniomandibular Disorders. 3 (4): 211–212.
PMID2639158.
^Wiedemann M, de Lima VM, Hanke W (April 1996). "Effects of antimigraine drugs on retinal spreading depression". Naunyn-Schmiedeberg's Archives of Pharmacology. 353 (5): 552–556.
doi:
10.1007/BF00169175.
PMID8740149.
S2CID6932302.
Iprazochrome is an
antimigraine agent used for prophylaxis of the attacks. It is also indicated for
diabetic retinopathy (both treatment and prevention in people with type-2 diabetes).
Chemically, it is a derivative of
adrenochrome, which is a product of
adrenaline oxidation. And it is a derivative of
carbazochrome as well.
This drug decreases the permeability and fragility of blood vessels, which reduces the number of migraine days and attenuates the symptoms associated with this condition, but it does not eliminate them altogether.
In animal models, iprazochrome was shown not to decrease the
spreading depression velocity, which is a feature of other antimigraine agents and is thought to be one of the essential causes of classical migraines.[2]
Dose
For migraines, 1-3 tabletes (each tablet contains 2.5 mg of iprazochrome) are taken three times a day. An abortive medication is recommended in the first weeks of treatment.
For diabetic retinopaty, 2 tablets are taken three times a day. If the initial treatment was successful, it can be reduced to 1 tablet three times a day.
The effect of this medication is usually seen after a month. It's achieves its full efficacy after 3 months of treatment.
Side effects
It can work as an anorectic and can cause skin allergic reactions after discontinuing.
This drug was also shown to induce pain in patients with atypical facial pain.[1]
Pharmacokinetics
Absorption
After taking the drug on empty stomach, it is rapidly absorbed. Peak serum concentration (
Cmax) is achieved after 1 hour, but its effect on blood vessels is seen only after 3 hours.
Elimination
The
half-life of iprazochrome is 2.2 hours. It is metabolised renally and 20% is eliminated in an unchanged form.
There are two known metabolites of iprazochrome: an
indole derivative (detected in urine) and a 6-hydroxy derivative (detected in feces).
References
^
abHampf G (1989). "Effect of serotonin antagonists on patients with atypical facial pain". Journal of Craniomandibular Disorders. 3 (4): 211–212.
PMID2639158.
^Wiedemann M, de Lima VM, Hanke W (April 1996). "Effects of antimigraine drugs on retinal spreading depression". Naunyn-Schmiedeberg's Archives of Pharmacology. 353 (5): 552–556.
doi:
10.1007/BF00169175.
PMID8740149.
S2CID6932302.