Damoral - General Information
A barbituric acid derivative that acts as a nonselective central nervous system depressant. It promotes binding to inhibitory gamma-aminobutyric acid subtype receptors, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations. [PubChem]
Pharmacology of Damoral
Damoral, the longest-acting barbiturate, is used for its anticonvulsant and sedative-hypnotic properties in the management of all seizure disorders except absence (petit mal).
Damoral for patients
Practitioners should give the following information and instructions to patients receiving barbiturates:
1. The use of phenobarbital carries with it an associated risk of psychological and/or physical dependence.
The patient should be warned against increasing the dose of the drug without consulting a physician.
2. Phenobarbital may impair mental and/or physical abilities required for the performance of potentially
hazardous tasks (e.g., driving, operating machinery, etc.).
3. Alcohol should not be consumed while taking phenobarbital. Concurrent use of phenobarbital with other
CNS depressants (e.g., alcohol, narcotics, tranquilizers, and antihistamines) may result in additional CNS
Most reports of clinically significant drug interactions occurring with the barbiturates have involved phenobarbital.
1. Anticoagulants: Phenobarbital lowers the plasma levels of dicumarol (name previously used: bishydorxycoumarin) and
causes a decrease in anticoagulant activity as measured by the prothrombin time. Phenobarbital can induce hepatic
microsomal enzymes resulting in increased metabolism and decreased anticoagulant response of oral anticoagulants (e.g.,
warfarin, acenocournarol, dicumarol, and phenprocoumon). Patients stabilized on anticoagulant therapy may require dosage
adjustments if phenobarbital is added to or withdrawn from their dosage regimen.
2. Corticosteroids: Phenobarbital appears to enhance the metabolism of exogenous corticosteroids probably through the
induction of hepatic microsomal enzymes. Patients stabilized on corticosteroid therapy may require dosage adjustments
if phenobarbital is added to or withdrawn from their dosage regimen.
3. Griseofulvin: Phenobarbital appears to interfere with the absorption of orally administered griseofulvin, thus
decreasing its blood level. The effect of the resultant decreased blood levels of griseofulvin on therapeutic response
has not been established. However, it would be preferable to avoid concomitant administration of these drugs.
4. Doxycycline: Phenobarbital has been shown to shorten the half- life of doxycycline for as long as 2 weeks after
barbiturate therapy is discontinued. This mechanism is probably through the induction of hepatic microsomal enzymes that
metabolize the antibiotic. If phenobarbital and doxycycline are administered concurrently, the clinical response to
doxycycline should be monitored closely.
5. Phenytoin, sodium valproate, valproic acid: The effect of phenobarbital on the metabolism of phenytoin appears to be
variable. Some investigators report an accelerating effect, while others report no effect. Because the effect of
phenobarbital on the metabolism of phenytoin is not predictable, phenytoin and phenobarbital blood levels should be
monitored more frequently if these drugs are given concurrently. Sodium valproate and valproic acid appear to decrease
phenobarbital metabolism; therefore, phenobarbital blood levels should be monitored and appropriate dosage adjustments
made as indicated.
6. Central nervous system depressants: The concomitant use of other central nervous system depressants including other
sedatives or hypnotics, antihistamines, tranquilizers, or alcohol, may produce additive depressant effects.
7. Monoamine oxidase inhibitors (MAOIs): MAOIs prolong the effects of phenobarbital probably because metabolism of the
phenobarbital is inhibited.
8. Estradiol, estrone, progesterone and other steroidal hormones: Pretreatment with or concurrent administration of
phenobarbital may decrease the effect of estradiol by increasing its metabolism. There have been reports of patients
treated with antiepileptic drugs (e.g., phenobarbital) who became pregnant while taking oral contraceptives. An alternate
contraceptive method might be suggested to women taking phenobarbital.
Phenobarbital is contraindicated in patients with known phenobarbital sensitivity or a history of manifest or
Additional information about Damoral
Damoral Indication: For the treatment of all types of seizures except absence seizures.
Mechanism Of Action: Damoral acts on GABAA receptors, increasing synaptic inhibition. This has the effect of elevating seizure threshold and reducing the spread of seizure activity from a seizure focus. Damoral may also inhibit calcium channels, resulting in a decrease in excitatory transmitter release. The sedative-hypnotic effects of phenobarbital are likely the result of its effect on the polysynaptic midbrain reticular formation, which controls CNS arousal.
Drug Interactions: Not Available
Food Interactions: Avoid alcohol.
Avoid excessive quantities of coffee or tea (Caffeine).
Increase dietary intake of magnesium, folate, vitamin B6, B12, and/or consider taking a multivitamin.
Generic Name: Phenobarbital
Synonyms: Phenobarbitol; Phenobarbituric Acid; Phenylethylbarbiturate; Phenylethylbarbituric Acid; Phenylethylmalonylurea; Fenobarbital
Drug Category: Hypnotics and Sedatives; Anticonvulsants
Drug Type: Small Molecule; Approved
Absorption: Absorbed in varying degrees following oral, rectal or parenteral administration. The salts are more rapidly absorbed than are the acids. The rate of absorption is increased if the sodium salt is ingested as a dilute solution or taken on an empty stomach.
Toxicity (Overdose): CNS and respiratory depression which may progress to Cheyne-Stokes respiration, areflexia, constriction of the pupils to a slight degree (though in severe poisoning they may wshow paralytic dilation), oliguria, tachycardia, hypotension, lowered body temperature, and coma. Typical shock syndrome (apnea, circulatory collapse, respiratory arrest, and death) may occur.
Protein Binding: 20 to 45%
Biotransformation: Hepatic (mostly via CYP2C19).
Half Life: 53 to 118 hours (mean 79 hours)
Dosage Forms of Damoral: Tablet Oral
Chemical IUPAC Name: 5-ethyl-5-phenyl-1,3-diazinane-2,4,6-trione
Chemical Formula: C12H12N2O3
Phenobarbital on Wikipedia: https://en.wikipedia.org/wiki/Phenobarbital
Organisms Affected: Humans and other mammals