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Kaythane Tablets

NAFDAC REG NO: B4-7820 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 29 October 2026 · synced automatically from official sources.
Produit
Kaythane Tablets
Numéro NAFDAC
B4-7820
Principe actif
Trihexyphenidyl Hydrochloride (Benzhexol Hydrochloride)
Dosage
5 mg
Forme
Tablet
Conditionnement
1 x 500's (in a jar)
Fabricant
Non répertorié
Déposant / Titulaire :
Kayhelt Pharma Limited
Approuvé
25 Jun 2025
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
24 Jun 2030
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

What we found

  • Kaythane Tablets is on the NAFDAC register with an active registration (B4-7820). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Kaythane Tablets

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

Trihexyphenidyl is indicated as an adjunct in the treatment of all forms of parkinsonism (postencephalitic, arteriosclerotic, and idiopathic). It is often useful as adjuvant therapy when treating these forms of parkinsonism with levodopa. Additionally, it is indicated for the control of extrapyramidal disorders caused by central nervous system drugs such as the dibenzoxazepines, phenothiazines, thioxanthenes, and butyrophenones.

Comment le prendre et à quelle fréquence
  • Dosage should be individualized
  • The initial dose should be low and then increased gradually, especially in patients over 60 years of age.Whether trihexyphenidyl may best be given before or after meals should be determined by the way the patient reacts
  • Postencephalitic patients, who are usually more prone to excessive salivation, may prefer to take it after meals and may, in addition, require small amounts of atropine which, under such circumstances, is sometimes an effective adjuvant
  • If trihexyphenidyl tends to dry the mouth excessively, it may be better to take it before meals, unless it causes nausea
  • If taken after meals, the thirst sometimes induced can be allayed by mint candies, chewing gum or water
  • Abrupt withdrawal of treatment for parkinsonism may result in acute exacerbation of parkinsonism symptoms; therefore, abrupt withdrawal should be avoided
  • Abrupt withdrawal of treatment may result in neuroleptic malignant syndrome (NMS) (See WARNINGS )
  • Idiopathic Parkinsonism As initial therapy for parkinsonism, 1 mg of trihexyphenidyl hydrochloride may be administered the first day
  • The dose may then be increased by 2 mg increments at intervals of three to five days, until a total of 6 to 10 mg is given daily
  • The total daily dose will depend upon what is found to be the optimal level
  • Many patients derive maximum benefit from this daily total of 6 to 10 mg, but some patients, chiefly those in the postencephalitic group, may require a total daily dose of 12 to 15 mg. …
Children
  • Safety and effectiveness
  • In pediatric patients have not been established. (See also ADVERSE REACTIONS )
Older adults

Sensitivity to the actions of parasympatholytic drugs may increase with age, particularly over the age of 60; therefore, elderly patients generally should be started on low doses of trihexyphenidyl and observed closely. Trihexyphenidyl has been shown to cause some cognitive dysfunctions in the elderly, including confusion and memory impairment. (See ADVERSE REACTIONS and DOSAGE AND ADMINISTRATION ).

While you are taking it
  • Trihexyphenidyl may impair mental and/or physical abilities required for performance of hazardous tasks, such as operating machinery or driving a motor vehicle
  • Patients should be cautioned about operating machinery, including automobiles, until they are reasonably certain that trihexyphenidyl therapy does not adversely affect their ability to engage in such activities
  • Because of increased sedative effects, patients should be cautioned to avoid the use of alcohol or other CNS depressants while taking trihexyphenidyl
  • Since this medication may increase the susceptibility to heat stroke (gastrointestinal (GI) problems, fever, heat intolerance), use with caution during hot weather. …
Talk to a doctor first if
  • Trihexyphenidyl is contraindicated in patients with hypersensitivity to trihexyphenidyl or to any of the other ingredients
  • Trihexyphenidyl is also contraindicated in patients with narrow angle glaucoma
  • Blindness after long-term use due to narrow angle glaucoma has been reported
Medicines it may not mix with

Cannabinoids, barbiturates, opiates, and alcohol may have additive effects with trihexyphenidyl, and thus, an abuse potential exists. Concurrent use of alcohol or other CNS depressants with trihexyphenidyl may cause increased sedative effects. Monoamine oxidase inhibitors and tricyclic antidepressants possessing significant anticholinergic activity may intensify the anticholinergic effects of antidyskinetic agents because of the secondary anticholinergic activities of these medications. Prophylactic administration of anticholinergic agents, such as trihexyphenidyl, as a prevention of drug-induced parkinsonism during neuroleptic therapy is not recommended. …

Warnings

Patients to be treated with trihexyphenidyl should have a gonioscope evaluation prior to initiation of therapy and close monitoring of intraocular pressures. The use of anticholinergic drugs may precipitate angle closure with an increase in intraocular pressure. If blurring of vision occurs during therapy, the possibility of narrow angle glaucoma should be considered. Blindness has been reported due to aggravation of narrow angle glaucoma. (See CONTRAINDICATIONS and ADVERSE REACTIONS ). …

Effets secondaires possibles

Minor side effects, such as dryness of the mouth, blurred vision, dizziness, mild nausea or nervousness, will be experienced by 30 to 50 percent of all patients. These sensations, however, are much less troublesome with trihexyphenidyl than with belladonna alkaloids and are usually less disturbing than unalleviated parkinsonism. Such reactions tend to become less pronounced, and even to disappear, as treatment continues. Even before these reactions have remitted spontaneously, they may often be controlled by careful adjustment of dosage form, amount of drug, or interval between doses. …

Pregnancy and breastfeeding

Pregnancy Teratogenic Effects Pregnancy Category C Animal reproduction studies to evaluate teratogenic and embryotoxic potential have not been conducted with trihexyphenidyl. It is also not known whether trihexyphenidyl can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Trihexyphenidyl should be given to a pregnant woman only if clearly needed.

If you take too much

The mean oral LD 50 of trihexyphenidyl has been reported to be 365 mg/kg (range, 325 to 410 mg/kg) in mice and 1660 mg/kg (1420 to 1940 mg/kg) in rats. At a dose of 40 mg/kg, dogs have exhibited emesis, restlessness followed by drowsiness, equilibrium disturbances, and mydriasis. In humans, doses up to 300 mg (5 mg/kg) have been ingested without fatalities or sequelae. However, rare cases of death associated with trihexyphenidyl overdosages taken in conjunction with other CNS-depressant agents have been reported or in patients with a compromised respiratory condition. …

Dépendance et mésusage

Although trihexyphenidyl is not classified as a controlled substance, the possibility of abuse should be borne in mind due to its stimulant and euphoriant properties.

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2022-06-21.

Label for trihexyphenidyl hydrochloride (benzhexol hydrochloride), the active ingredient registered with NAFDAC.

Check your pack of Kaythane Tablets

Add the expiry date on your pack for a full Trust Score.

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Encore 3 vérifications gratuites aujourd'hui Sources officielles : FDA américaine · EMA (UE) · NAFDAC · alertes OMS

About Kaythane Tablets

What is in Kaythane Tablets?

Kaythane Tablets contains Trihexyphenidyl Hydrochloride (Benzhexol Hydrochloride) (5 mg), as tablet, according to its NAFDAC registration record.

Is Kaythane Tablets registered with NAFDAC?

Yes. Kaythane Tablets is listed on the NAFDAC register under registration number B4-7820, and its registration is active as of 29 October 2026.

Has Kaythane Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Kaythane Tablets in our automatically synced alert list.

How can I check that my pack of Kaythane Tablets is genuine?

Run a free authenticity scan with the NAFDAC number B4-7820, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Kaythane Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Dosage should be individualized. The initial dose should be low and then increased gradually, especially in patients over 60 years of age.Whether trihexyphenidyl may best be given before or after meals should be determined by the way the patient reacts. Postencephalitic patients, who are usually more prone to excessive salivation, may prefer to take it after meals and may, in a…

What is Kaythane Tablets used for?

Trihexyphenidyl is indicated as an adjunct in the treatment of all forms of parkinsonism (postencephalitic, arteriosclerotic, and idiopathic). It is often useful as adjuvant therapy when treating these forms of parkinsonism with levodopa. Additionally, it is indicated for the control of extrapyramidal disorders caused by central nervous system drugs such as the dibenzoxazepines, phenothiazines, th (Summarised from the official U.S. FDA label for trihexyphenidyl hydrochloride (benzhexol hydrochloride). Always follow your doctor or pharmacist.)

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