Desmotabs Melt 240 micrograms oral lyophilisate

  • Name:

    Desmotabs Melt 240 micrograms oral lyophilisate

  • Company:
    info
  • Active Ingredients:

    Desmopressin Acetate

  • Legal Category:

    Product subject to medical prescription which may be renewed (B)

Summary of Product Characteristics last updated on medicines.ie: 30/11/2020

Click on this link to Download PDF directly

Ferring Ireland Limited

Ferring Ireland Limited

Company Products

Medicine NameActive Ingredients
Medicine Name Cortiment 9mg prolonged release tablets Active Ingredients Budesonide
Medicine Name DDAVP Desmopressin 100 micrograms/ml Nasal drops,solution Active Ingredients Desmopressin Acetate
Medicine Name DDAVP/Desmopressin 4 micrograms/ml Solution for Injection Active Ingredients Desmopressin Acetate
Medicine Name Desmospray, Desmopressin Nasal Spray Active Ingredients Desmopressin Acetate
Medicine Name Desmotabs Melt 120 micrograms oral lyophilisate Active Ingredients Desmopressin Acetate
Medicine Name Desmotabs Melt 240 micrograms oral lyophilisate Active Ingredients Desmopressin Acetate
Medicine Name Desmotabs Melt 60 micrograms oral lyophilisate Active Ingredients Desmopressin Acetate
Medicine Name FIRMAGON 120 mg powder and solvent for solution for injection Active Ingredients degarelix acetate
Medicine Name FIRMAGON 80 mg powder and solvent for solution for injection Active Ingredients degarelix acetate
Medicine Name Glypressin 1 mg Powder and Solvent for Solution for Injection Active Ingredients Terlipressin acetate
Medicine Name Glypressin 1 mg/ 8.5 ml solution for injection Active Ingredients Terlipressin acetate
Medicine Name Gonapeptyl Depot 3.75 mg powder and solvent for suspension for injection Active Ingredients triptorelin acetate
Medicine Name Lutinus 100 mg Vaginal Tablets Active Ingredients Progesterone
Medicine Name Menopur 1200IU powder and solvent for solution for injection Active Ingredients Menotrophin
Medicine Name Menopur 600IU powder and solvent for solution for injection Active Ingredients Menotrophin
Medicine Name Menopur 75IU Powder and Solvent for Solution for Injection. Menotrophin (HMG) Active Ingredients Menotrophin
Medicine Name Noqturina 25 microgram oral lyophilisate Active Ingredients Desmopressin Acetate
Medicine Name Noqturina 50 microgram oral lyophilisate Active Ingredients Desmopressin
Medicine Name Nordurine 0.1 mg Tablets Active Ingredients Desmopressin Acetate
Medicine Name Nordurine 0.2mg Tablets Active Ingredients Desmopressin Acetate
Medicine Name Pabal 100 micrograms/ml solution for injection Active Ingredients Carbetocin
Medicine Name Pentasa 1 g Prolonged-release Tablets Active Ingredients Mesalazine
Medicine Name Pentasa 1 g Suppositories Active Ingredients Mesalazine
Medicine Name Pentasa 10 mg/ml Rectal Suspension Active Ingredients Mesalazine
Medicine Name Pentasa 500 mg Prolonged Release Tablets Active Ingredients Mesalazine
1 - 0 of 35 items.Total: Infinity pages

When a pharmaceutical company changes any document, a new version is published on medicines.ie. For each version, we show the dates it was published on medicines.ie and the reasons for change.

Updated on 30 November 2020

Reasons for updating

  • Change to Section 4.8 – Undesirable effects - how to report a side effect
  • Change to section 6.5 - Nature and contents of container

Free text change information supplied by the pharmaceutical company

Update to SPC Section 4.8 - Change to HPRA contact details

Update to SPC Section 6.5 - Deletion of 10-tablet pack size

Updated on 26 May 2015

Reasons for updating

  • New SmPC for new product

Legal category: Product subject to medical prescription which may be renewed (B)

Updated on 26 May 2015 SPC

Reasons for updating

  • Change to Section 4.8 – Undesirable effects - how to report a side effect

Legal category: Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

Update to include new HPRA contact information

Updated on 26 May 2015 PIL

Reasons for updating

  • Change to Section 4.8 – Undesirable effects - how to report a side effect

Free text change information supplied by the pharmaceutical company

Update to include new HPRA contact information

Updated on 16 December 2014 PIL

Reasons for updating

  • Correction of spelling/typing errors

Free text change information supplied by the pharmaceutical company

SPC unchanged.
Spelling error corrected.

Updated on 16 December 2014 SPC

Reasons for updating

  • Correction of spelling/typing errors

Legal category: Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

SPC unchanged.
Spelling error corrected.

Updated on 14 May 2013 SPC

Reasons for updating

  • Change to section 4.2 - Posology and method of administration
  • Change to section 4.4 - Special warnings and precautions for use
  • Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
  • Change to section 4.6 - Pregnancy and lactation
  • Change to section 4.8 - Undesirable effects
  • Change to section 5.1 - Pharmacodynamic properties
  • Change to section 5.2 - Pharmacokinetic properties
  • Change to section 5.3 - Preclinical safety data

Legal category: Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

Section 4.2: section ‘General’ inserted containing the following text:

Method of administration: Desmotabs Melt is placed under the tongue where it dissolves without the need for water.

 Effect of food: Food intake may reduce the intensity and duration of the antidiuretic effect at low doses of desmopressin (see section 4.5).

 In the event of signs or symptoms of water retention and /or hyponatraemia (headache, nausea/vomiting, weight gain, and, in severe cases, convulsions) treatment should be interrupted until the patient has fully recovered.  When restarting treatment strict fluid restriction should be enforced (see section 4.4).

 If adequate clinical effect is not achieved within 4 weeks following appropriate dose titration the medication should be discontinued.”

 

Section 4.2: ‘Special Population’ section inserted as follows:

“Elderly:

The initiation of treatment in the elderly (patients over 65 years) is contraindicated in patients being treated for nocturia and primary nocturnal enuresis.

Dosage recommendation for elderly suffering from central diabetes insipidus is the same as for other age groups. 

 

Renal Impairment

Desmotabs Melt is contraindicated in case of moderate and severe renal insufficiency (creatinine clearance below 50 ml/min) (see section 4.3).

 

Hepatic Impairment

In vitro human liver microsome metabolism studies of desmopressin have shown that no significant amount is metabolized in the liver by the cytochrome P450 system. Thus human liver metabolism in vivo by the cytochrome P450 system is unlikely to occur. The effect of desmopressin on the pharmacokinetics of other drugs is likely to be minimal due to its lack of inhibition of the cytochrome P450 drug metabolizing system (see section 4.5).

 

Paediatric Population

Desmotabs Melt is indicated in Central Diabetes Insipidus and Primary Nocturnal Enuresis (see section 5.1 and indication specific information in 4.2 above).  Dose recommendations are the same as in adults.”

 

Section 4.4:
-          sentence added:All patients and, when applicable, their guardians should be carefully instructed to adhere to the fluid restrictions. “
-          two statements added to the section ‘Precautions’:
    
o    “Precautions must be taken in patients at risk for increased intracranial pressure.”
    
o    “Desmopressin should be used with caution in patients with conditions characterized by fluid and/or electrolyte imbalance”

 

 

Section 4.5:
sentence updated as follows:

“Substances, which are known to induce SIADH, e.g. tricyclic antidepressants, selective serotonine reuptake inhibitors, chlorpromazine and carbamazepine as well as some antidiabetics of the sulfonylurea group particularly Chlorpropamide may cause an additive antidiuretic effect leading to an increased risk of water retention/hyponatraemia (see section 4.4).”


Section 4.6:
-          Sentence updated as follows: “Data on a limited number (n=53) of exposed pregnancies in women with diabetes insipidus as well as data on a limited number (n=54) of exposed pregnancies in women with von Willebrand disease indicate no adverse effects of desmopressin on pregnancy or on the health of the foetus/ newborn child.”

-          New sentences added:
    
o    “Caution should be exercised when prescribing Desmotabs Melt to pregnant women.”
    
o    “Fertility studies have not been done.  In vitro analysis of human cotyledon models have shown that there is no transplacental transport of desmopressin when administered at therapeutic concentrations corresponding to recommended dose.”


Section 4.8:
Full section update – see SPC for details.

Section 5.1:
Sentence updated as follows: “This results in a considerably longer duration of action and a complete lack of pressor effect in the dosages clinically used. The uterotonic and vasopressor actions are extremely low in the dosages clinical used.


Section 5.2:
full update, see SPC.


Section 5.3:
Section update as follows: “There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the SPCNon-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, toxicity to reproduction. Carcinogenicity studies have not been performed with desmopressin, because it is very closely related to the naturally-occurring peptide hormone.


Updated on 14 May 2013 PIL

Reasons for updating

  • Change to section 4.2 - Posology and method of administration
  • Change to section 4.4 - Special warnings and precautions for use
  • Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
  • Change to section 4.6 - Pregnancy and lactation
  • Change to section 4.8 - Undesirable effects
  • Change to section 5.1 - Pharmacodynamic properties
  • Change to section 5.2 - Pharmacokinetic properties
  • Change to section 5.3 - Preclinical safety data

Free text change information supplied by the pharmaceutical company

Section 4.2: section ‘General’ inserted containing the following text:

Method of administration: Desmotabs Melt is placed under the tongue where it dissolves without the need for water.

 Effect of food: Food intake may reduce the intensity and duration of the antidiuretic effect at low doses of desmopressin (see section 4.5).

 In the event of signs or symptoms of water retention and /or hyponatraemia (headache, nausea/vomiting, weight gain, and, in severe cases, convulsions) treatment should be interrupted until the patient has fully recovered.  When restarting treatment strict fluid restriction should be enforced (see section 4.4).

 If adequate clinical effect is not achieved within 4 weeks following appropriate dose titration the medication should be discontinued.”

 

Section 4.2: ‘Special Population’ section inserted as follows:

“Elderly:

The initiation of treatment in the elderly (patients over 65 years) is contraindicated in patients being treated for nocturia and primary nocturnal enuresis.

Dosage recommendation for elderly suffering from central diabetes insipidus is the same as for other age groups. 

 

Renal Impairment

Desmotabs Melt is contraindicated in case of moderate and severe renal insufficiency (creatinine clearance below 50 ml/min) (see section 4.3).

 

Hepatic Impairment

In vitro human liver microsome metabolism studies of desmopressin have shown that no significant amount is metabolized in the liver by the cytochrome P450 system. Thus human liver metabolism in vivo by the cytochrome P450 system is unlikely to occur. The effect of desmopressin on the pharmacokinetics of other drugs is likely to be minimal due to its lack of inhibition of the cytochrome P450 drug metabolizing system (see section 4.5).

 

Paediatric Population

Desmotabs Melt is indicated in Central Diabetes Insipidus and Primary Nocturnal Enuresis (see section 5.1 and indication specific information in 4.2 above).  Dose recommendations are the same as in adults.”

 

Section 4.4:
-          sentence added:All patients and, when applicable, their guardians should be carefully instructed to adhere to the fluid restrictions. “
-          two statements added to the section ‘Precautions’:
    
o    “Precautions must be taken in patients at risk for increased intracranial pressure.”
    
o    “Desmopressin should be used with caution in patients with conditions characterized by fluid and/or electrolyte imbalance”

 

 

Section 4.5:
sentence updated as follows:

“Substances, which are known to induce SIADH, e.g. tricyclic antidepressants, selective serotonine reuptake inhibitors, chlorpromazine and carbamazepine as well as some antidiabetics of the sulfonylurea group particularly Chlorpropamide may cause an additive antidiuretic effect leading to an increased risk of water retention/hyponatraemia (see section 4.4).”


Section 4.6:
-          Sentence updated as follows: “Data on a limited number (n=53) of exposed pregnancies in women with diabetes insipidus as well as data on a limited number (n=54) of exposed pregnancies in women with von Willebrand disease indicate no adverse effects of desmopressin on pregnancy or on the health of the foetus/ newborn child.”

-          New sentences added:
    
o    “Caution should be exercised when prescribing Desmotabs Melt to pregnant women.”
    
o    “Fertility studies have not been done.  In vitro analysis of human cotyledon models have shown that there is no transplacental transport of desmopressin when administered at therapeutic concentrations corresponding to recommended dose.”


Section 4.8:
Full section update – see SPC for details.

Section 5.1:
Sentence updated as follows: “This results in a considerably longer duration of action and a complete lack of pressor effect in the dosages clinically used. The uterotonic and vasopressor actions are extremely low in the dosages clinical used.


Section 5.2:
full update, see SPC.


Section 5.3:
Section update as follows: “There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the SPCNon-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, toxicity to reproduction. Carcinogenicity studies have not been performed with desmopressin, because it is very closely related to the naturally-occurring peptide hormone.


Updated on 25 January 2012 PIL

Reasons for updating

  • Change to section 4.8 - Undesirable effects
  • Change to section 4.3 - Contraindications
  • Change to section 4.4 - Special warnings and precautions for use
  • Change to section 6.3 - Shelf life
  • Change to section 6.4 - Special precautions for storage

Free text change information supplied by the pharmaceutical company

Sec 4.3: Statement added: “Before prescribing Desmotabs Melt the diagnoses of psychogenic polydipsia and alcohol abuse should be excluded.”

 

Sec 4.4: Statement added: “All patients on desmopressin therapy should be observed for the signs of symptoms associated with hyponatraemia (headache, nausea/vomiting, weight increased and, in severe cases, convulsions).”

 

Sec 4.8: Updated to MedDra format

 

Sec 6.3: Shelf-life updated from 3 to 4 years

 

Sec 6.4: Storage conditions updated to “Store in original package in order to protect from light and moisture”.

Updated on 25 January 2012 SPC

Reasons for updating

  • Change to section 4.8 - Undesirable effects
  • Change to section 4.3 - Contraindications
  • Change to section 4.4 - Special warnings and precautions for use
  • Change to section 6.3 - Shelf life
  • Change to section 6.4 - Special precautions for storage

Legal category: Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

Sec 4.3: Statement added: “Before prescribing Desmotabs Melt the diagnoses of psychogenic polydipsia and alcohol abuse should be excluded.”

 

Sec 4.4: Statement added: “All patients on desmopressin therapy should be observed for the signs of symptoms associated with hyponatraemia (headache, nausea/vomiting, weight increased and, in severe cases, convulsions).”

 

Sec 4.8: Updated to MedDra format

 

Sec 6.3: Shelf-life updated from 3 to 4 years

 

Sec 6.4: Storage conditions updated to “Store in original package in order to protect from light and moisture”.

Updated on 17 August 2010 PIL

Reasons for updating

  • New SPC for new product

Free text change information supplied by the pharmaceutical company

None provided

Updated on 17 August 2010 SPC

Reasons for updating

  • New SPC for new product

Legal category: Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

None provided