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Anusol HC® Suppositories
Staff Characteristics
Clinical Details
Registered Midwife
Clinical Situation for which
medicine is to be used
For the symptomatic relief of internal haemorrhoids and pruritus ani.
Clinical Criteria for inclusion
Postnatal women ≥ 16 years requiring management of the discomfort
associated with internal haemorrhoids and pruritus ani.
Clinical Criteria for exclusion
•
•
•
Known hypersensitivity to any component of the medicine.
Individuals< 16 years of age.
Women suffering from any of the following tubercular, fungal
and most viral lesions including herpes simplex, vaccinia and
varicella.
Management of excluded women
and those not wishing to receive
care
•
•
Refer to medical staff as appropriate.
Document action / refusal in woman’s maternity handheld
record or community notes.
Use in pregnancy or lactation
Use in pregnancy only when there is no safer alternative and when the
disease itself carries risks for the mother or child. Can be used in
lactation
Cautions and/or reasons for
seeking further advice from a
doctor
•
•
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•
Woman fits exclusion criteria.
Woman suffers an adverse drug reaction.
Chronic dosing is required.
Woman declines medication.
Cautions and action that will be
taken if a caution applies
•
•
Check for and document any allergies.
Check and document past medical and drug history and current
medication to ascertain potential for overdose.
If a caution applies consult with a doctor.
Document consultation in woman’s maternity handheld record
or community notes.
Refer to current BNF for latest information on interactions.
•
•
•
Description of Treatment
Name / Form / Strength of
Medicine
Anusol HC / Suppositories
Dosage
One suppository
Route of administration
Rectal
Frequency of administration
Morning and night and after each evacuation
Duration of treatment
48 Hours
Legal Status
•
P – midwife may supply
Storage requirements
Do not store above 25°C
Warnings
Following symptomatic relief, definitive diagnosis should be
established.
Follow –up
•
•
Refer if woman develops side/adverse effects or if there is an
inadequate response.
Refer immediately in case of overdose.
Undesirable effects
Prolonged or excessive use may produce systemic corticosteroid
effects, and use for periods longer than seven days is not
recommended. Rarely, there are sensitivity reactions. Patients may
occasionally experience transient burning on application, especially if
the anoderm is not intact
• If a serious adverse reaction is suspected please report to the
MHRA Yellow Card Scheme http://yellowcard.mhra.gov.uk/
Overdose
If swallowed, fever, nausea, vomiting, stomach cramps and diarrhoea
may develop 3-12 hours after ingestion.Hydrocortisone normally does
not produce toxic effects in an acute single overdose. Treatment of a
large acute overdose should include gastric lavage, purgation with
magnesium sulphate and complete bed rest. If necessary, give oxygen
and general supportive measures. Methaemoglobinaemia should be
treated by intravenous methylthioninium chloride
• Immediate assessment / treatment is essential – refer to
medical staff.
• Manage in accordance with established treatment guidelines or
see BNF overdose section.
• For further advice contact National Poisons Centres
0844 892 0111.
Advice to be given to the woman
•
•
•
•
Explain treatment and course of action.
Side effects explained.
Verbal consent obtained before administration.
It is good practice to offer the woman the manufacturer’s
Patient Information Leaflet to support any verbal advice
provided.
Monitoring arrangements during
and after treatment and follow-up
required.
•
If thewoman suffers a serious adverse drug reaction, seek
immediate medical assistance.
Monitor for side effects and effectiveness.
To be reviewed by doctor if inadequate response.
Records to be kept
References
•
•
Must be written in the once only medicines and pre-medications
section of the medicine kardex. The person who writes up the
medication must write their designation after their signature e.g.
Midwife Band (*).Also record the administration, date, time and name
of practitioner in the relevant section of the woman’s maternity
handheldrecord or community notes.
•
•
BNF 67
Anusol HC ® Suppositories SPC 10th March 2008
www.medicines.org.uk