1. What is DESMOPRESSIN and What
Is It Used For?
DESMOPRESSIN is a synthetic analogue of arginine
vasopressin (AVP), the body's natural antidiuretic hormone (ADH). Desmopressin
acts on V2 receptors in the kidney collecting ducts, increasing water
reabsorption and reducing urine output without the vasopressor (blood pressure
raising) effects of natural vasopressin.
Desmopressin 0.2 mg tablets are indicated for:
· primary nocturnal
enuresis (bedwetting) in children and adults;
· central diabetes
insipidus — a condition caused by insufficient ADH production from the
pituitary gland, resulting in the production of large volumes of dilute urine;
· polyuria/polydipsia
associated with central (not nephrogenic) diabetes insipidus.
In von Willebrand disease type 1 and mild haemophilia A,
desmopressin transiently releases stored von Willebrand factor and factor VIII
from endothelial cells, helping to control minor bleeding. (This is typically
managed with IV or intranasal formulations rather than the tablet form.)
2. How to Take This Medicine
Nocturnal
Enuresis (Bedwetting)
• Children (5 years and
above) and adults: 0.1 mg (1 tablet) taken 1 hour before bedtime.
Central
Diabetes Insipidus
• Initial: 0.05 to 0.2 mg
once daily at bedtime.
• May adjust bedtime
dosage in 0.05 mg increments, if needed, to control nocturia, up to 1.2 mg/day
administered in 2 or 3 divided doses.
Important
Administration Instructions
Tablets should be swallowed whole with water. For nocturnal
enuresis, fluid intake must be restricted from 1 hour before taking the dose
until 8 hours after — this is essential to prevent dangerous hyponatraemia (low
sodium). Drink only small sips of water with the tablet.
3. Side Effects
Common
Side Effects
• Headache.
• Nausea and abdominal
discomfort.
• Nasal congestion (more
common with intranasal forms).
Serious
Side Effect — Hyponatraemia (Low Blood Sodium)
The most important and potentially dangerous side effect is
hyponatraemia (low serum sodium), caused by excessive water retention. This is
especially likely if fluid restriction is not observed. Symptoms include:
• Headache, nausea,
vomiting.
• Confusion,
irritability, drowsiness.
• Seizures or loss of
consciousness (severe cases — medical emergency).
If symptoms of hyponatraemia occur, stop desmopressin
immediately and seek urgent medical attention.
4. Contraindications — Who
Should NOT Take This Medicine
|
Do not take DESMOPRESSIN if you: •
You have habitual or psychogenic polydipsia (compulsive
water drinking). •
You have cardiac insufficiency or other conditions
requiring diuretic therapy. •
You have known hyponatraemia (low blood sodium). •
You have nephrogenic diabetes insipidus (kidney does not
respond to ADH — desmopressin will not work). •
You have syndrome of inappropriate ADH secretion (SIADH). •
You are under 5 years old (for nocturnal enuresis
indication). •
You are allergic to desmopressin or any tablet component. |
5. Safety Warnings and Special
Precautions
Fluid
Restriction is Mandatory
For nocturnal enuresis, patients must not drink more than
240 mL (one glass) from 1 hour before the dose until 8 hours after.
Non-adherence to this rule is the primary cause of dangerous hyponatraemia.
Parents/caregivers must be thoroughly counselled on this restriction.
Electrolyte
Monitoring
Measure serum sodium before starting therapy and at regular
intervals during treatment, especially in elderly patients, young children, and
those with conditions predisposing to electrolyte disturbance. If serum sodium
falls below 130 mmol/L, stop treatment and restrict fluids.
Elderly
Patients
Older adults are particularly vulnerable to hyponatraemia
due to reduced renal concentrating ability and often higher fluid intake. Extra
caution and more frequent electrolyte monitoring is required in this
population.
Intercurrent
Illness
During acute illness (especially with vomiting, diarrhoea,
or fever), desmopressin therapy should be temporarily suspended and fluid
management reviewed, as electrolyte disturbances are more likely.
6. Drug Interactions
• Non-steroidal
anti-inflammatory drugs (NSAIDs — ibuprofen, diclofenac) — enhance antidiuretic
effect and increase risk of hyponatraemia; use with caution.
• Tricyclic
antidepressants (e.g., imipramine, amitriptyline) — increase antidiuretic
effect.
• Carbamazepine,
chlorpropamide — potentiate antidiuretic effect; increased hyponatraemia risk.
• Loperamide — increases
desmopressin plasma levels by approximately threefold; dose adjustment may be
needed.
• Indomethacin —
increases renal sensitivity to desmopressin.
• Diuretics — may
antagonise the antidiuretic effect.
7. Storage Instructions
• Store below 30 degrees
Celsius.
• Keep dry — protect from
moisture.
• Keep in original
blister packaging.
• Keep out of reach of
children.
• Do not use after the
expiry date printed on the pack.
8. Prescription Status in Kenya
Desmopressin 0.2 mg tablets are a prescription-only
medicine (POM) in Kenya, available through authorised pharmacies with a valid
prescription from a registered medical practitioner.
It is used across general practice, paediatrics,
endocrinology, and nephrology settings.
9. Patient Guidance
|
Important Reminders for Patients •
Always restrict fluid intake from 1 hour before your
bedtime dose until the next morning — this is the most important rule to stay
safe. •
If you or your child develops a headache, confusion,
nausea, or feel unusually drowsy after taking the tablet, seek medical
attention immediately. •
Do not skip your scheduled follow-up appointments — blood
sodium levels need to be checked during treatment. •
Do not give this medicine to children under 5 years for
bedwetting. •
If your child is unwell with vomiting, diarrhoea, or
fever, stop the medicine and contact your doctor. •
This medicine does not work for bedwetting caused by
kidney problems — if in doubt, ask your doctor. |
10. Pharmacist / Prescriber
Notes
Electrolyte
Monitoring Schedule
• Serum sodium: before
initiation, at 7 days, 1 month, then 3-monthly during chronic therapy.
• Action threshold:
discontinue if Na+ falls below 130 mmol/L.
• More frequent
monitoring in the elderly (monthly), young children, and patients on concomitant
NSAIDs or antidepressants.
Treatment
Withdrawal
After 3 months of treatment, assess dry night frequency. If
successful, gradually taper and trial off. Reassess after a 1-week washout. If
dryness is maintained, discontinue. If bedwetting recurs, reinstate for a further
3 months, then repeat assessment.
Paediatric
Counselling Key Points
Counsel parents explicitly on the fluid restriction rule, document this counselling. Advise limiting fluid intake after 5 pm. Provide a
written information sheet. Ensure alarm bells are used adjunctively when
possible for enuresis.
Diabetes
Insipidus Titration
Start low (0.1 mg twice or three times daily) and titrate
based on 24-hour urine volume and osmolality. Target: urine osmolality >300
mOsm/kg. Avoid over-suppression (risk of hyponatraemia); accept some polyuria
if electrolytes are marginal.
11. Frequently Asked Questions
(FAQs)
How long will my child need to take this medicine for
bedwetting?
Treatment is usually given for 3 months at a time. After
that, your doctor will review whether it is still needed. Some children achieve
lasting dryness after one course; others may need longer treatment. The
medicine is not a permanent cure, but helps control the problem while the child
matures.
Can my child drink normally during the day while on this
medicine?
Yes — normal daytime fluid intake is encouraged and
important for hydration. The restriction only applies from 1 hour before the
bedtime dose until the next morning (8 hours). During the day, drinks should be
unrestricted.
What happens if I forget to restrict fluids before the
bedtime dose?
If fluid intake is not restricted, there is a risk of water
retention and dangerously low blood sodium (hyponatraemia). If this occurs,
symptoms include headache, confusion, and in severe cases, seizures. On any
night where fluid restriction is not possible, it is safer to skip the dose and
take it the next night.
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