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   » » Wiki: Cyclizine
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Cyclizine, sold under a number of brand names, is a medication used to treat and prevent , and due to or . It may also be used for nausea after general anaesthesia or that which developed from use.

(2026). 9781455749898, Elsevier Health Sciences. .
It is taken by mouth, in the , or .

Common side effects include sleepiness, dry mouth, , and trouble with vision. More serious side effects include low blood pressure and urinary retention. It is not generally recommended in young children or those with . Cyclizine appears to be safe during but has not been well studied. It is in the and family of medications.

Cyclizine was discovered in 1947.

(2026). 9781899163922, JJG. .
It is on the World Health Organization's List of Essential Medicines. In the United States it is available over the counter.


Medical uses
Primary uses include , and associated with , vertigo and post-operatively following administration of general anesthesia and . It is sometimes given in hyperemesis gravidarum, although the manufacturer advises that it be avoided in pregnancy. Off-license use often occurs with specialists in hospitals to treat inpatients who have become severely dehydrated in pregnancy. An off-label use is as an opioid/opiate potentiator.

The drug Diconal is a combination of cyclizine and the opioid . Dipipanone is a schedule I controlled substance in the US.


Contraindications
Its antimuscarinic action warrants caution in patients with prostatic hypertrophy, urinary retention, or angle-closure . Liver disease exacerbates its effects.


Adverse effects
Common (over 10%) — , .

Uncommon (1% to 10%) — Headache, psychomotor impairment, dermatitis, and effects such as diplopia (double vision), , , urinary retention and gastro-intestinal disturbances.

Rare (less than 1%) — Hypersensitivity reactions (, , , rashes and reactions), extrapyramidal effects, dizziness, confusion, depression, sleep disturbances, , liver dysfunction, and .


Pharmacology
Cyclizine is a derivative with histamine H1-receptor antagonist () activity. The precise mechanism of action in inhibiting the symptoms of motion sickness is not well understood. It may have effects directly on the vestibular system and on the chemoreceptor trigger zone. Cyclizine exerts a central () action.


Synthesis
Cyclizine may be prepared by the Eschweiler–Clarke methylation of diphenylmethylpiperazine or by reaction of benzhydryl bromide with 1-methylpiperazine in acetonitrile to form the hydrobromide salt of the drug.


History
Cyclizine was developed in the American division of pharmacy company Burroughs Wellcome (today ) during a research study involving many drugs of the antihistamine group. Cyclizine was quickly clinically found as a potent and long-acting antiemetic. The company named the substance – or more precisely cyclizine's form which it usually appears in – "marezine hydrochloride" and started to sell it in the United States under trade name Marezine. Selling was begun in under trade name Marzine in 1965.
(2026). 9780471899792, John Wiley & Sons. .
(1988). 9780815511441, William Andrew. .

The substance received more credit when chose it as a space antiemetic for the first crewed Moon flight. Cyclizine was introduced to many countries as a common antiemetic. It is an over-the-counter drug in many countries because it has been well tolerated, although it has not been studied much.


Society and culture
Some people using methadone recreationally combine cyclizine with their dose, a combination that is known to produce strong effects. It has also been used recreationally for its effects to induce hallucinations.

It has been used illegally in to sabotage a dog's performance.Conor Ryan for The Independent. June 20, 2013 IGB left with €250k bill after dog doping case


Names
As cyclizine hydrochloride tablets and cyclizine lactate solution for intramuscular or intravenous injection (brand names: Valoid in UK and South Africa and Marezine, Marzine and Emoquil in US). Cyclizine was marketed as Bonine for Kids in the US, but was discontinued in 2012, and replaced with meclizine.


Cyclizine derivatives
Cyclizine
CH3
Cl
Cl
H
Cl
Cl


See also


External links
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