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Boehringer Ingelheim Limited Consumer Healthcare

Ellesfield Avenue, Bracknell, Berkshire, RG12 8YS
Telephone: +44 (0)1344 424 600
Fax: +44 (0)1344 741 399
WWW: http://www.boehringer-ingelheim.co.uk
Medical Information Direct Line: +44 (0)1344 741 286
Medical Information e-mail: medinfo@bra.boehringer-ingelheim.com
Customer Care direct line: +44 (0)1344 741 186
Medical Information Fax: +44 (0)1344 741 298

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Summary of Product Characteristics last updated on the eMC: 17/06/2011
SPC DULCOLAX Tablets, 5mg

When a pharmaceutical company changes an SPC or PIL, a new version is published on the eMC. For each version, we show the dates it was published on the eMC and the reasons for change.

Updated on 17/06/2011 and displayed until Current
Reasons for adding or updating:
  • Change to section 1 -Name of the Medicinal product
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-May-2011
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company

Medicinal product name amended from "Dulolax Tablets 5 mg" to "Dulcolax 5 mg Gastro-resistant Tablets"

Date of Revision amended.
Updated on 10/02/2011 and displayed until 17/06/2011
Reasons for adding or updating:
  • Change to section 4.2 - Posology and method of administration
  • Change to section 5.2 - Pharmacokinetic Properties
Date of revision of text on the SPC:   01-Oct-2010
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company

Section 4.2
Consequential changes to section 4.2.

Section 5.2
Section 5.2 has been extensively updated.
Updated on 09/11/2010 and displayed until 10/02/2011
Reasons for adding or updating:
  • Change to section 10 date of revision of the text
  • Change to section 4.6 - Pregnancy and Lactation
  • Change to section 4.7 - Effects on Ability to Drive and Use Machines
  • Change to section 4.8 - Undesirable Effects
Date of revision of text on the SPC:   01-Oct-2010
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Section 4.6 Pregnancy and Lactation

A new final (now fourth) paragraph has been added regarding the conduction of studies on the effect on human fertility.

 

Section 4.7 Effects on Ability to Drive and Use Machines

A new final (now second) paragraph has been added regarding vasovagal response and dizziness and/or syncope.

 

Section 4.8 Undesirable Effects

A new first paragraph has been added entitled “The most commonly reported adverse events …”.

 

The text “Not known – incidence cannot be estimated from the available data” has been deleted from after the “Adverse events have been ranked under headings of frequency …” paragraph.

 

All Immune System Disorders now come under the “Rare” heading.  The “Not known” heading has been deleted from the Immune System Disorders paragraph.

 

The text “Not known” has been replaced with the text “Rare” in the Metabolism and Nutrition Disorders paragraph.

 

A new paragraph regarding Nervous System Disorders has been added to this section.

 

The colitis listing in the Gastrointestinal Disorders paragraph has been changed from “Not known” to “Rare”.  The “Not known” text has been deleted.

 

Section 10 Date of Revision of the Text

The date has been updated from August 2010 to October 2010. 

Updated on 01/09/2010 and displayed until 09/11/2010
Reasons for adding or updating:
  • Change to section 5.1 - Pharmacodynamic Properties
  • Change to section 5.2 - Pharmacokinetic Properties
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-Aug-2010
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Section 5.1 Pharmacodynamic Properties

Text has been both added to and deleted from this section to align with Company Core Data Sheet.

 

Section 5.2 Pharmacokinetic Properties

Text has been both added to and deleted from this section to align with Company Core Data Sheet.

 

Section 10 Date of Revision of the Text

The date has been updated to August 2010.

Updated on 24/05/2010 and displayed until 01/09/2010
Reasons for adding or updating:
  • Change to section 4.7 - Effects on Ability to Drive and Use Machines
  • Change to section 6. 6 - Instructions for use, handling and disposal
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-May-2010
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Section 4.7 Effects on Ability to Drive and Use Machines

The previous text of:

 

DULCOLAX has no effect on ability to drive and use machinery.

 

has been replaced with the following text:

 

No studies on the effects of DULCOLAX on the ability to drive and use machines have been performed.

 

Section 6.6 Special Precautions for Disposal

The header for this section has been amended from:

 

Instructions for use/handling

 

to:

 

Special precautions for disposal

 

Section 10 Date of Revision of the Text

The date has been updated to May 2010.

Updated on 16/04/2010 and displayed until 24/05/2010
Reasons for adding or updating:
  • Change to section 10 date of revision of the text
  • Change to section 4.2 - Posology and method of administration
Date of revision of text on the SPC:   01-Mar-2010
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Section 4.2 Posology and Method of Administration

Text for the entire section has been reworded and replaced, with the exception of the two paragraphs commencing with the following:

 

When using DULCOLAX to prepare the patient for radiographic examination …

 

and

 

No specific information on the use of this product is the elderly is available …

 

which remain as before.

 

Section 10 Date of Revision of the Text

The date has been updated to March 2010.

Updated on 12/03/2010 and displayed until 16/04/2010
Reasons for adding or updating:
  • Change to section 4.4 - Special warnings and precautions for Use
  • Change to section 4.6 - Pregnancy and Lactation
  • Change to section 4.8 - Undesirable Effects
  • Change to section 4.9 - Overdose
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-Mar-2010
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Section 4.4 Special Warnings and Special Precautions for Use

New third and fourth paragraphs have been inserted as follows:

 

Third paragraph now starts with Intestinal loss of fluids can promote dehydration.

 

Fourth paragraph now starts with Patients may experience haematochezia (blood in stool) that is generally mild and self-limiting.

 

What is now the fifth paragraph (that starting with Dizziness and/or syncope…) has had text both deleted from and added to.

 

Section 4.6 Pregnancy and Lactation

What used to be the second paragraph has been deleted i.e. text There is no evidence as to whether bisacodyl is excreted into breast milk.

 

A new second paragraph has been inserted which now starts with the text Clinical data show that neither the active moiety of bisacodyl …

 

Section 4.8 Undesirable Effects

The text Rare: hypersensitivity has been added to the Immune system disorders.

 

The text … neurotic o… and … and other hypersensitivity has been deleted from the Not known paragraph in Immune system disorders.

 

A whole new paragraph regarding Metabolism and nutrition disorders has been added.

 

The text …, haematochezia (blood in stool), abdominal discomfort, anorectal discomfort has been added to the Uncommon paragraph in Gastrointestinal disorders.

 

The text … abdominal discomfort has been deleted from the Common paragraph in Gastrointestinal disorders.

 

Section 4.9 Overdose

The words watery stools, brackets either side of the word diarrhoea and word fluid have all been added to the first paragraph of the Symptoms section.

 

Text (including reference to gastric lavage) has both been deleted from and added to the Therapy section.

 

Section 10 Date of Revision of the Text

The date has been updated from January 2009 to March 2010.

 

Updated on 02/02/2009 and displayed until 12/03/2010
Reasons for adding or updating:
  • Change to section 4.6 - Pregnancy and Lactation
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-Jan-2009
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Dulcolax Tablets P SPC changes

 

Section 4.6 Pregnancy and Lactation

The words … adequate and well-controlled studies in pregnant women.  Long experience has shown no evidence of undesirable or damaging effects during pregnancy have been added to the first paragraph of this section.

 

The words … reports of undesirable or damaging effects during pregnancy or to the foetus attributable to the use of DULCOLAX have been deleted from the first paragraph of this section.

 

The words There is no evidence as to whether bisacodyl is excreted into breast milk have been added as a new second paragraph.

 

In what was previously the second paragraph of this section, the following text has been deleted:

 

used

to the foetus

 

In what was previously the second paragraph of this section, the following text has been added:

 

as with all

DULCOLAX

taken

and during breast feeding

and only on medical advice

 

The following text has been deleted (from what was previously the third paragraph):

 

Although the active ingredient of DULCOLAX is not known to be excreted in breast milk, its use during breast feeding is not recommended.

 

Section 10 Date of Revision of the Text

The date has been updated to January 2009.

 

Updated on 23/12/2008 and displayed until 02/02/2009
Reasons for adding or updating:
  • Change to section 4.4 - Special warnings and precautions for Use
  • Change to section 4.8 - Undesirable Effects
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-Dec-2008
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Dulcolax Tablets P SPC changes

  

Section 4.4 – Special Warnings and Precautions for Use

The text “There have been isolated reports of abdominal pain and bloody diarrhoea occurring after taking bisacodyl.  Some cases have been shown to be associated with colonic mucosal ischaemia.” has been added as a new fourth paragraph.

 

Section 4.8 – Undesirable Effects

The whole of this section has been removed and replaced with the following text:

 

“Adverse events have been ranked under headings of frequency using the following convention: Very common (≥ 1/10); common (≥ 1/100, < 1/10); uncommon (≥ 1/1000, <1/100); rare (≥ 1/10000, <1/1000); very rare (<1/10000).

Not known – incidence cannot be estimated from the available data.

 

Immune system disorders

Not known: anaphylactic reactions, angioneurotic oedema and other hypersensitivity.

 

Gastrointestinal disorders

Uncommon: vomiting.

Common: Abdominal discomfort, abdominal pain, abdominal cramps, nausea and diarrhoea.

Not known: colitis.”

 

Section 10 – Date of revision of the text:

The date has been updated to December 2008.

 

Updated on 10/12/2008 and displayed until 23/12/2008
Reasons for adding or updating:
  • Change to section 4.4 - Special warnings and precautions for Use
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-Nov-2008
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Section 4.4 – Special Warnings and Precautions for Use

 

The word “daily” has been added between the words “continuous” and “basis” of the first paragraph.

 

The words “without investigating the cause of constipation” have been added at the end of the first paragraph i.e. after the words “… more than five days”.

 

The words “If laxatives are needed every day, the cause of constipation should be investigated” have been deleted as the second paragraph.

 

The words “and may precipitate onset of rebound constipation” have been deleted from what was the third paragraph.

 

The words “Children under 10 years should not take DULCOLAX without medical advice” have been deleted from what was the fifth paragraph and the words “DULCOLAX should not be taken by children under 10 years without medical advice” added.

 

The words “DULCOLAX Tablets contain a small amount of lactose (33.2 mg) and sucrose (23.4 mg) in each tablet” have been added as the first sentence of what was the sixth paragraph.

  

Section 10 – Date of revision of the text:

 

The date has been updated to November 2008.

Updated on 10/09/2008 and displayed until 10/12/2008
Reasons for adding or updating:
  • Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
  • Change to section 10 date of revision of the text
  • Change to section 4.9 - Overdose
Date of revision of text on the SPC:   01-Aug-2008
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



Dulcolax Tablets (P) SPC changes

 

 

Section 4.5 – Interactions

 

The word “medicaments” has been deleted from the header of this section and the words “medicinal products” added.

 

The words “if excessive doses of DULCOLAX are taken” has been added to the second paragraph and the words “However, this situation only arises if excessive doses of DULCOLAX are taken (See Overdose Section)” deleted.

 

The words “Electrolyte imbalance may lead to increased sensitivity to cardiac glycosides” have been added as a third paragraph.

 

Section 4.9 – Overdose:

 

The words “This may also lead to increased sensitivity to cardiac glycosides” have been deleted from the “Symptoms” paragraph.

 

The words “Laxatives when taken in” have been added to paragraph 2.  The words “with laxatives” have been deleted from the first sentence of paragraph 2.

 

Section 10 – Date of revision of the text:

 

The words “July 2008” have been replaced with the words “August 2008”.

Updated on 29/08/2008 and displayed until 10/09/2008
Reasons for adding or updating:
  • Change to section 4.3 - Contraindications
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-Jul-2008
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company

Section 4.3:

DULCOLAX is contraindicated must not be used in patients with ileus, intestinal obstruction, acute surgical abdominal conditions including such as acute appendicitis, acute inflammatory bowel diseases, and severe abdominal pain associated with nausea and vomiting which may be indicative of the aforementioned severe conditions.

in severe dehydration.

DULCOLAX is also contraindicated in severe dehydration and in patients with a known hypersensitivity to bisacodyl or any other component of ingredient in the product.

Section 10
Revision date amended

Updated on 17/03/2008 and displayed until 29/08/2008
Reasons for adding or updating:
  • Change to section 6.1 - List of Excipients
  • Change to section 6. 3 - Shelf Life
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   05/2007
Legal Category:   P
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company

Sections 6.1 and 6.3, as well as the revision date have been amended as follows:

Section 6.1 List of excipients removal of the excipient dibutyl phthalate and replacement with castor oil

Section 6.3 Shelf life reduction of the shelf life to 3 years

Updated on 15/08/2007 and displayed until 17/03/2008
Reasons for adding or updating:
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   03/2006
Legal Category:   POM
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company

Change to date of revision
Updated on 27/06/2005 and displayed until 15/08/2007
Reasons for adding or updating:
  • Change to section 4.4 - Special Warnings and Precautions for Use
  • Change to section 6. 5 - Nature and Contents of Container
  • Change to section 10 (date of (partial) revision of the text
Updated on 27/08/2003 and displayed until 27/06/2005
Reasons for adding or updating:
  • Change to section 2 - qualitative and quantitative composition
  • Change to section 3 - pharmaceutical form
  • Change to section 4.1 - Therapeutic Indications
  • Change to section 4.2 - Posology and Method of Administration
  • Change to section 5.2 - Pharmacokinetic Properties
  • Change to section 6. 5 - Nature and Contents of Container
Updated on 27/08/2003 and displayed until 27/08/2003
Reasons for adding or updating:
  • New SPC for eMC ie an SPC for an existing product, but one that is new for the eMC
Updated on 16/08/2001 and displayed until 27/08/2003
Reasons for adding or updating:
  • Change to section 6. 4 - Special Precautions for Storage
Updated on 09/07/2001 and displayed until 16/08/2001
Reasons for adding or updating:
  • Change to section 4.3 - Contra-indications
  • Change to section 4.4 - Special Warnings and Precautions for Use
  • Change to section 4.8 - Undesirable Effects
  • Change to section 4.9 - Overdose
Updated on 18/01/2000 and displayed until 09/07/2001
Reasons for adding or updating:
  • No reasons supplied

Active Ingredients/Generics

 
   bisacodyl