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New search Medicine profile Pyridostigmine

Clinical medicine profile

Pyridostigmine

Therapeutic agent (verify pharmacological class)

POM
Evidence state Source-linked Review date not recorded
Route
See product SmPC
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
01 Risk first

Safety essentials

The information most likely to change a prescribing or dispensing decision.

Contraindications

  • CONTRAINDICATIONS Pyridostigmine bromide tablets are contraindicated in mechanical intestinal or urinary obstruction, and particular caution should be used in its administration to patients with bronchial asthma.
  • Care should be observed in the use of atropine for counteracting side effects, as discussed below.

Precautions

  • WARNINGS Although failure of patients to show clinical improvement may reflect underdosage, it can also be indicative of overdosage.
  • As is true of all cholinergic drugs, overdosage of pyridostigmine bromide may result in cholinergic crisis, a state characterized by increasing muscle weakness which, through involvement of the muscles of respiration, may lead to death.
  • Myasthenic crisis due to an increase in the severity of the disease is also accompanied by extreme muscle weakness, and thus may be difficult to distinguish from cholinergic crisis on a symptomatic basis.
  • Such differentiation is extremely important, since increases in doses of pyridostigmine bromide or other drugs of this class in the presence of cholinergic crisis or of a refractory or "insensitive" state could have grave consequences.
  • Osserman and Genkins 1 indicate that the differential diagnosis of the two types of crisis may require the use of Tensilon TM (edrophonium chloride) as well as clinical judgment.
  • The treatment of the two conditions obviously differs radically.
  • Whereas the presence of myasthenic crisis suggests the need for more intensive anticholinesterase therapy, the diagnosis of cholinergic crisis, according to Osserman and Genkins 1 calls for the prompt withdrawal of all drugs of this type.
  • The immediate use of atropine in cholinergic crisis is also recommended.
  • Atropine may also be used to abolish or obtund gastrointestinal side effects or other muscarinic reactions
  • but such use, by masking signs of overdosage, can lead to inadvertent induction of cholinergic crisis.
  • For detailed information on the management of patients with myasthenia gravis, the physician is referred to one of the excellent reviews such as those by Osserman and Genkins 2 , Grob 3 or Schwab 4,5 .
  • Usage in Pregnancy The safety of pyridostigmine bromide during pregnancy or lactation in humans has not been established.
02 Point of care

Dosing matrix

Population and organ-function guidance, shown together for faster comparison.

Adult

DOSAGE AND ADMINISTRATION Each Pyridostigmine Bromide Tablet contains 60 mg pyridostigmine bromide. Dosage The size and frequency of the dosage must be adjusted to the needs of the individual patient. The average dose is ten 60 mg tablets daily, spaced to provide maximum relief when maximum strength is needed. In severe cases as many as twenty-five tablets a day may be required, while in mild cases one to six tablets a day may suffice. NOTE: For information on a diagnostic test for myasthenia gravis, and for the evaluation and stabilization of therapy, please see product literature on Tensilon (edrophonium chloride).

Paediatric

Pediatric Use Safety and effectiveness in pediatric patients have not been established.

Renal

Review renal impairment dosing; many agents need CrCl/eGFR adjustment.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.
Hepatic

Review hepatic impairment dosing; monitor LFTs if agent is hepatically cleared or hepatotoxic.

03 Clinical use

Use, effects & interactions

Indications

  • Myasthenia gravis, paroxysmal tachycardia, migraine and intestinal and post-operative atony, termination of effects of neuromuscular blocking agent Clinical selection for Pyridostigmine should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Therapeutic agent (verify pharmacological class).
  • Confirm site-specific dose, duration and monitoring before prescribing.

Adverse effects

  • ADVERSE REACTIONS The side effects of pyridostigmine bromide are most commonly related to overdosage and generally are of two varieties, muscarinic and nicotinic.
  • Among those in the former group are nausea, vomiting, diarrhea, abdominal cramps, increased peristalsis, increased salivation, increased bronchial secretions, miosis and diaphoresis.
  • Nicotinic side effects are comprised chiefly of muscle cramps, fasciculation and weakness.
  • Muscarinic side effects can usually be counteracted by atropine, but for reasons shown in the preceding section the expedient is not without danger.
  • As with any compound containing the bromide radical, a skin rash may be seen in an occasional patient.
  • Such reactions usually subside promptly upon discontinuance of the medication.
  • To report SUSPECTED ADVERSE REACTIONS, contact ANI Pharmaceuticals, Inc. at 1-855-204-1431 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
  • Professional use: confirm indication, dose, duration, monitoring and patient counselling points against current Kenya STG / EML and the product SmPC.
  • Document allergy status and key interactions.
04 Pharmacology

Mechanism & disposition

It inhibits the hydrolysis of acetylcholine by competing with it for attachment to acetylcholinesterase at sites of cholinergic transmission.

It inhibits the hydrolysis of acetylcholin…It has some direct cholinergic activity.
Read complete mechanism

It inhibits the hydrolysis of acetylcholine by competing with it for attachment to acetylcholinesterase at sites of cholinergic transmission. It has some direct cholinergic activity.

Onset

Product-specific

Duration

Product-specific

Route

See product SmPC

05 Special populations

Pregnancy, lactation & diet

Pregnancy

Usage in Pregnancy The safety of pyridostigmine bromide during pregnancy or lactation in humans has not been established. Therefore, use of pyridostigmine bromide in women who may become pregnant requires weighing the drug's potential benefits against its possible hazards to mother and child.

Lactation

Assess infant risk vs benefit of maternal therapy; prefer agents with lactation data.

06 Kenya market

Brands & loaded prices

From
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BrandManufacturerPackObserved price
No reviewed brand listings are linked yet.
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; FDA drug label via OpenFDA/DailyMed; Professional class pharmacology (Therapeutic agent (verify pharmacological class))
Last reviewedNot recorded
EvidenceSource-linked
Open source document ↗

Decision support only. Confirm patient-specific decisions against the current product SmPC, Kenya STG/EML, and professional judgement.