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Emixol Tablets

NAFDAC Reg. No. A4-101439 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Emixol Tablets
NAFDAC number
A4-101439
Active ingredient
Trihexyphenidyl Hydrochloride (Benzhexol Hydrochloride)
Strength
5 mg
Form
Tablet
Pack size
1 x 500's (in LDPE bag)
Manufacturer
Not listed
Applicant (holder)
Eminent Drugs and Pharmaceuticals Ltd
Approved
30 Jul 2025
Status
Active View on NAFDAC ↗
Registration valid to
29 Jul 2030
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Emixol Tablets is on the NAFDAC register with an active registration (A4-101439). 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 Emixol Tablets

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is 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, thioxanthenes, and butyrophenones.

How to take it and how often
  • 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
  • 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 ). …

Possible side effects

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. …

Dependence and misuse

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.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

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 Emixol Tablets

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Emixol Tablets

What is in Emixol Tablets?

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

Is Emixol Tablets registered with NAFDAC?

Yes. Emixol Tablets is listed on the NAFDAC register under registration number A4-101439, and its registration is active as of 28 October 2026.

Has Emixol Tablets been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number A4-101439, 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 Emixol 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 Emixol 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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