CONCERTA XL 18 mg prolonged-release tablets
*Company:
Janssen Sciences Ireland (a Johnson & Johnson Company)Status:
No Recent UpdateLegal Category:
Product subject to medical prescription which may not be renewed (A)Active Ingredient(s):
*Additional information is available within the SPC or upon request to the company
Updated on 09 November 2022
File name
PI-Concerta XL-18mg-Ireland-English-IAIN_111.pdf
Reasons for updating
- Change to section 4.8 - Undesirable effects
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
DE/H/6007/001-004/IA/111 - Update EUPI following PRAC recommendation - EoP 2-November-2022
Updated on 09 November 2022
File name
PIL-Concerta XL-18-36 mg-Ireland-English-IAIN_111.pdf
Reasons for updating
- Change to section 4 - possible side effects
- Change to section 6 - date of revision
Free text change information supplied by the pharmaceutical company
DE/H/6007/001-004/IA/111 - Update EUPI following PRAC recommendation - EoP 2-Nov-22
Updated on 05 August 2022
File name
PI-Concerta XL-18mg-Ireland-English-II_107.pdf
Reasons for updating
- Change to section 4.1 - Therapeutic indications
- 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 6.6 - Special precautions for disposal and other handling
- Change to section 10 - Date of revision of the text
- Change to improve clarity and readability
Legal category:Product subject to medical prescription which may not be renewed (A)
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DE_H_6007_001-004_II_107_ Adult de novo Indication
Updated on 05 August 2022
File name
PIL-Concerta XL-18-36 mg-Ireland-English-II_107.pdf
Reasons for updating
- Change to section 1 - what the product is used for
- Change to section 2 - what you need to know - warnings and precautions
- Change to section 3 - how to take/use
- Change to section 4 - possible side effects
- Change to section 6 - date of revision
- Changes to therapeutic indications
Free text change information supplied by the pharmaceutical company
DE_H_6007_001-004_II_107_ Adult de novo Indication
Updated on 16 May 2022
File name
PI-Concerta-18mg-Ireland-English-DE_H_6007_001-004_IA_104_consolidated_II_92.pdf
Reasons for updating
- Other
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Correction to add back 2 missing paragraphs which already had been approved.
Section 4.4:
Use with serotonergic medicinal products
Serotonin syndrome has been reported following coadministration of methylphenidate with serotonergic medicinal products. If concomitant use of methylphenidate with a serotonergic medicinal product is warranted, prompt recognition of the symptoms of serotonin syndrome is important. These symptoms may include mental‑status changes (e.g., agitation, hallucinations, coma), autonomic instability (e.g., tachycardia, labile blood pressure, hyperthermia), neuromuscular abnormalities (e.g., hyperreflexia, incoordination, rigidity), and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhoea). Methylphenidate must be discontinued as soon as possible if serotonin syndrome is suspected.
Section 4.5:
Use with serotonergic medicinal products
There have been reports of serotonin syndrome following coadministration of methylphenidate with serotonergic medicinal products. If concomitant use of methylphenidate with a serotonergic medicinal product is warranted, prompt recognition of the symptoms of serotonin syndrome is important (see section 4.4). Methylphenidate must be discontinued as soon as possible if serotonin syndrome is suspected.
Updated on 12 October 2020
File name
SPC-Concerta-18mg-Ireland-English-DE_H_6007_001-004_IA_104_EDMS-ERI-138444855_11.0-C25-7Oct2020-cl.pdf
Reasons for updating
- Change to section 4.8 - Undesirable effects
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 12 October 2020
File name
PIL-Concerta-18-36 mg-Ireland-English-DE_H_6007_001-004_IA_104_EDMS-ERI-183377703_8.0-7Oct2020-cl.pdf
Reasons for updating
- Change to section 4 - possible side effects
- Change to section 4 - how to report a side effect
- Change to section 6 - date of revision
Updated on 09 September 2020
File name
IE-Concerta-PIL 18_36mg.pdf
Reasons for updating
- Change to section 2 - excipient warnings
- Change to section 6 - date of revision
Free text change information supplied by the pharmaceutical company
Concerta XL contains sodium
This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium‑free’.
Updated on 05 August 2020
File name
CONCERTA 18 XL_Tablet, Film Coated, Extended Release clean.pdf
Reasons for updating
- Change to section 2 - Qualitative and quantitative composition
- Change to section 4.4 - Special warnings and precautions for use
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
update in line with excipient guideline
Updated on 12 April 2019
File name
IE-Concerta-PIL-18-36mg-Brexit-clean.pdf
Reasons for updating
- Change to section 4 - how to report a side effect
- Change to section 6 - marketing authorisation holder
- Change to section 6 - date of revision
Updated on 12 April 2019
File name
IE-Concerta-SmPC-18mg-C22-29mar19-Brexit-clean.pdf
Reasons for updating
- Change to section 7 - Marketing authorisation holder
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 06 March 2019
File name
UK-IE-Concerta-PIL-18-36-54mg-II092-clean.pdf
Reasons for updating
- Change to section 2 - interactions with other medicines, food or drink
- Change to section 6 - date of revision
Updated on 06 March 2019
File name
IE-Concerta XL-SmPC-18mg-C21-II092-Clean.pdf
Reasons for updating
- 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 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
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CCDS Dec 2016 (092) safety change
Updated on 17 July 2018
File name
PIL-Concerta XL-18-36-54mg-C20-11jul18-clean.pdf
Reasons for updating
- Change to section 6 - what the product contains
- Change to section 6 - date of revision
Updated on 17 July 2018
File name
Concerta XL-IE-SmPC-18mg-C20-11jul18-clean.pdf
Reasons for updating
- Change to section 6.1 - List of excipients
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
6.1 List of excipients
Butylhydroxytoluene (E321)
Cellulose acetate
Hypromellose (E464)
Phosphoric acid concentrated
Poloxamer 188
Polyethylene oxides 200K and 7000K
Povidone K29-32
Sodium chloride
Stearic acid
Succinic acid
Iron oxide black (E172)
Iron oxide yellow (E172)
Film Coat
Iron oxide yellow (E172)
Hypromellose (E464)
Lactose monohydrate
Stearic acid
Titanium dioxide (E171)
Triacetin
Clear Coat
Carnauba wax
Hypromellose (E464)
Macrogol 400
Printing Ink
Iron oxide black (E172)
Hypromellose (E464)
Isopropyl alcohol
Propylene glycol
Purified water
Updated on 19 February 2018
Reasons for updating
- New SPC for new product
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 19 February 2018
File name
PIL_9209_403.pdf
Reasons for updating
- New PIL for new product
Updated on 19 February 2018
File name
PIL_9209_403.pdf
Reasons for updating
- New PIL for new product
Updated on 19 February 2018
Reasons for updating
- 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 5.2 - Pharmacokinetic properties
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
4.4 Special warnings and precautions for use
Aggressive or hostile behaviour
The emergence or worsening of aggression or hostility can be caused by treatment with stimulants. Aggression has been reported in patients treated with methylphenidate (see section 4.8). Patients treated with methylphenidate should be closely monitored for the emergence or worsening of aggressive behaviour or hostility at treatment initiation, at every dose adjustment and then at least every 6 months and every visit. Physicians should evaluate the need for adjustment of the treatment regimen in patients experiencing behaviour changes bearing in mind that upwards or downwards titration may be appropriate. Treatment interruption can be considered.
Anxiety, agitation or tension
Anxiety, agitation and tension have been reported in patients treated with methylphenidate (see section 4.8). Methylphenidate is also associated with the worsening of pre-existing anxiety, agitation or tension, and anxiety led to discontinuation of methylphenidate in some patients. Clinical evaluation for anxiety, agitation or tension should precede use of methylphenidate and patients should be regularly monitored for the emergence or worsening of these symptoms during treatment, at every adjustment of dose and then at least every 6 months or every visit.
4.6 Fertility, pregnancy and lactation
Methylphenidate has been found in the breast-milk of a woman treated with methylphenidate. Methylphenidate is excreted in human milk. Based on reports of breast milk sampling from five mothers, methylphenidate concentrations in human milk resulted in infant doses of 0.16% to 0.7% of the maternal weight‑adjusted dosage, and a milk to maternal plasma ratio ranging between 1.1 and 2.7.
5.2 Pharmacokinetic properties
Replacement of (0-inf) with inf throughout
Updated on 19 February 2018
Reasons for updating
- Change to section 2 - what you need to know - warnings and precautions
- Change to section 2 - interactions with other medicines, food or drink
- Change to section 2 - pregnancy, breast feeding and fertility
- Change to section 4 - possible side effects
- Change to section 4 - how to report a side effect
- Change to section 6 - date of revision
- Correction of spelling/typing errors
Updated on 19 April 2017
Reasons for updating
- Correction of spelling/typing errors
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Updated on 20 March 2017
Reasons for 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
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Inclusion of the following wording on Priapism in Section 4.4:
Priapism
Prolonged and painful erections have been reported in association with methylphenidate products, mainly in association with a change in the methylphenidate treatment regimen. Patients who develop abnormally sustained or frequent and painful erections should seek immediate medical attention.
Addition of Priapism, Erection increased and Prolonged erection as adverse reaction with 'not known' frequency in Section 4.8.
Updated on 17 March 2017
Reasons for updating
- Change to section 2 - what you need to know - warnings and precautions
- Change to section 4 - possible side effects
- Change to section 6 - date of revision
Updated on 18 May 2016
Reasons for updating
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.8
Addition of
Hepatobiliary disorders –very rare- acute hepatic failure
Other ADR changes =changed system organ class
System Organ Class |
Adverse |
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Frequency |
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Very common |
Common |
Uncommon |
Rare |
Very rare |
Not known |
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Psychiatric disorders* |
Insomnia, Nervousness |
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Psychotic disorders*, Auditory, visual and tactile hallucination*, Anger, Suicidal ideation*, Mood altered, Restlessness†, Tearfulness, Worsening of pre-existing tics of Tourette’s syndrome*, Logorrhoea, Hypervigilance, Sleep disorder |
Mania*†, Disorientation, Libido disorder, Confusional state† |
Suicidal attempt (including completed suicide)* †, Transient depressed mood*, Abnormal thinking, Apathy†, Repetitive behaviours, Over-focussing |
Delusions*†, Thought disturbances*, dependence. Cases of abuse and dependence have been described, more often with immediate release formulations |
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Hepatobiliary disorders |
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Alanine aminotransferase increased# |
Hepatic enzyme |
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Abnormal liver function, including acute hepatic failure and hepatic coma, Blood alkaline phosphatase increased, Blood bilirubin increased† |
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Investigations |
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Changes in blood pressure and heart rate (usually an increase)*, Weight decreased* |
Cardiac murmur* |
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* See section 4.4 # Frequency derived from adult clinical trials and not on data from trials in children and adolescents; may also be relevant for children and adolescents. † Frequency derived from clinical trials in children and adolescent and reported at a higher frequency in clinical trials in adult patients. |
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Updated on 17 May 2016
Reasons for updating
- Change to side-effects
- Change to date of revision
Updated on 20 July 2015
Reasons for updating
- Change to section 4.1 - Therapeutic indications
- Change to section 4.2 - Posology and method of administration
- Change to section 4.3 - Contraindications
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 4.9 - Overdose
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Update to section 4.1, 4.2, 4.3 (admin)
Update to section 4.8 _ ADR reporting statement
Update to section 4.9 (overdose)
Treatment
There is no specific antidote to methylphenidate overdosage.
Treatment consists of appropriate supportive measures.
The patient must be protected against self-injury and against external stimuli that would aggravate overstimulation already present. . If the signs and symptoms are not too severe and the patient is conscious, gastric contents may be evacuated by induction of vomiting or gastric lavage. Before performing gastric lavage, control agitation and seizures if present and protect the airway. Other measures to detoxify the gut include administration of activated charcoal and a cathartic. In the presence of severe intoxication, a carefully titrated dose of a benzodiazepine be given before performing gastric lavage The efficacy of activated charcoal has not been established.
Updated on 17 July 2015
Reasons for updating
- Change to date of revision
- Addition of information on reporting a side effect.
Updated on 04 September 2014
Reasons for updating
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.7:
When early discharge is envisaged, patients should be advised not to drive or operate machinery for the 24 hours following administration.
This medicine can impair cognitive function and can affect a patient’s ability to drive safely. When prescribing this medicine, patients should be told:
• The medicine is likely to affect your ability to drive
• Do not drive until you know how the medicine affects you
• It may be an offence to drive while under the influence of this medicine
Updated on 02 September 2014
Reasons for updating
- Change to information about driving or using machinery
- Change to date of revision
Updated on 04 March 2013
Reasons for 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
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.5 Interaction:
Use with centrally acting alpha‑2 agonists (e.g. clonidine)
Serious adverse events, including sudden death, have been reported in concomitant use with clonidine.
The long-term safety of using methylphenidate in combination with clonidine or other centrally acting alpha‑2 agonists has not been systematically evaluated.
Updated on 28 November 2012
Reasons for updating
- Change to side-effects
- Change to date of revision
Updated on 27 November 2012
Reasons for updating
- Change to section 4.8 - Undesirable effects
- Change to section 9 - Date of renewal of authorisation
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.8
Addition of “ logorrhoea” under Psychiatric Disorders~ uncommon and “pollakiura” under renal and urinary disorders ~uncommon
Updated on 14 September 2011
Reasons for updating
- Change to section 4.4 - Special warnings and precautions for use
- Change to section 4.9 - Overdose
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Aggressive or hostile behaviour
The emergence or worsening of aggression or hostility can be caused by treatment with stimulants. Patients treated with methylphenidate should be closely monitored for the emergence or worsening of aggressive behaviour or hostility at treatment initiation, at every dose adjustment and then at least every 6 months and every visit. Physicians should evaluate the need for adjustment of the treatment regimen in patients experiencing behaviour changes bearing in mind that upwards or downwards titration may be appropriate. Treatment interruption can be considered.
Section 4.9 Overdose
When treating patients with overdose, allowances must be made for the delayed release of methylphenidate from this formulations with extended durations of action
Updated on 16 August 2011
Reasons for updating
- Correction of spelling/typing errors
Updated on 27 June 2011
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 4.8 - Undesirable effects
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
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under 'Adults' change to advice to allow continuation into adulthood.
Now states; 'In adolescents whose symptoms persist into adulthood and who have shown clear benefit from treatment, it may be appropriate to continue treatment into adulthood. However, start of treatment with CONCERTA XL in adults is not appropriate (see sections 4.4 and 5.1).'
Section 4.4 Special warnings and precautions:
Use in adults . text update to :' Safety and efficacy have not been established for the initiation of treatment in adults or the routine continuation of treatment beyond 18 years of age. If treatment withdrawal has not been successful when an adolescent has reached 18 years of age continued treatment into adulthood may be necessary. The need for further treatment of these adults should be reviewed regularly and undertaken annually.
Cardiovascular status: 'The possibility of clinical complications cannot be excluded as a result of the effects observed in the clinical trial data especially when treatment during childhood/adolescence is continued into adulthood.
Section 4.8 Undesirable effects Addition of adverse events seen in adult clinical trials.
Section 5.1 Pharmacodynamics: addition of adult clinical trial efficacy data (18 to 65 years)
Updated on 24 June 2011
Reasons for updating
- Change to, or new use for medicine
- Change to side-effects
- Change to date of revision
Updated on 10 November 2010
Reasons for updating
- Change to section 4.2 - Posology and method of administration
- Change to section 4.8 - Undesirable effects
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.8 _ no addtional adverse effects chnage in frequency of several ADRS
Updated on 01 November 2010
Reasons for updating
- Change to side-effects
Updated on 11 March 2010
Reasons for updating
- 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 4.7 - Effects on ability to drive and use machines
- Change to section 4.8 - Undesirable effects
- Change to section 4.9 - Overdose
- Change to section 5.3 - Preclinical safety data
- Change to section 10 - Date of revision of the text
- Change to section 4.1 - Therapeutic indications
- Change to section 4.2 - Posology and method of administration
- Change to section 4.3 - Contraindications
- Change to section 4.4 - Special warnings and precautions for use
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
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4.1 |
Therapeutic Indications |
Treatment must be under the supervision of a specialist in childhood behavioural disorder, and emphasis on the need for remedial measures before introducing pharmacotherapy. |
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4.2 |
Posology and method of administration |
Addition of Phaecochromocytoma |
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4.3 |
Contraindications |
Addition of Phaecochromocytoma |
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4.4 |
Special Warnings and Precautions for Use |
More detailed information on long term effects, ongoing monitoring requirements, and withdrawing medication for trial period |
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4.5 |
Interaction with other medicinal products and other forms of interaction |
Additional caution with dopaminergic drugs, clonidine, halogenated anaesthetics , antihypertensive drugs |
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4.6 |
Pregnancy and Lactation |
Pregnancy:Addition of reports of neonatal cardioresipiratory toxicity, specifically foetal tachycardia and respiratory distress Lactation: methylphenidate has been found in breast milk, one case report of weight decrease |
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4.7 |
Effects of ability to drive and use machines |
Visual disturbances including blurred vision may affect ability to drive or operate machinery |
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4.8 |
Undesirable effects |
Table has been re-formatted with new system organ classes.In crease in number and type of psychiatric side effects including suicide. Also reports of cerebrovascular accident , neuroleptics malignant syndrome, choreoatheroid movements, hyperhidrosis, muscle cramps, gynaecomastia |
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4.9 |
Overdose |
No new information section re-written |
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5.3 |
Preclinical Safety Data |
No new information section re-written |
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10. |
DATE OF REVISION OF THE TEXT |
Changed to Ferbruary 2010
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Updated on 08 February 2010
Reasons for updating
- Change to warnings or special precautions for use
- Change of contraindications
- Change to side-effects
- Change to drug interactions
- Change to date of revision
- Change due to user-testing of patient information
Updated on 12 February 2009
Reasons for updating
- Introduction of new strength
- Change to section 8 - MA number
- Change to section 9 - Date of renewal of authorisation
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
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New SPC for new product |
New Strength of Concerta XL |
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8. |
MARKETING AUTHORISATION NUMBER(S) |
PA 748/49/4 |
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9. |
DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION |
01 August 08 |
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10. |
DATE OF REVISION OF THE TEXT |
August 08 |
Updated on 12 February 2009
Reasons for updating
- SPC re-instated
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Updated on 12 February 2009
Reasons for updating
- PIL re-instated
Updated on 01 September 2008
Reasons for updating
- Change to section 7 - Marketing authorisation holder
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
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7. |
MARKETING AUTHORISATION HOLDER
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Update address to 50-100 Holmers Farm Way |
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10. |
DATE OF REVISION OF THE TEXT |
Changed to August 2008 |
Updated on 28 August 2008
Reasons for updating
- Addition of marketing authorisation holder
Updated on 17 October 2007
Reasons for 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
- Change to separate SPCs covering individual presentations
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
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Change to section 4.4 – Special Warnings and Precautions for Use |
Addition of mania/aggression sub-headings & text |
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Change to section 4.8 – Undesirable effects |
Major revision to update to 2005 SPC guidance |
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Change to section 10 – Date of revision of the text |
Changed to September 2007 |
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Change to separate SPCs covering individual presentations |
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Updated on 17 October 2007
Reasons for updating
- Change to warnings or special precautions for use
- Change to side-effects
- Change to date of revision
Updated on 03 September 2007
Reasons for updating
- Change due to harmonisation of patient information leaflet
- Change due to user-testing of patient information
Updated on 27 July 2007
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 6.1 - List of excipients
- Change to section 6.6 - Special precautions for disposal and other handling
- Change to section 9 - Date of renewal of authorisation
- Change to section 10 - Date of revision of the text
- Change to joint SPC covering all presentations
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
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Change to section 4.2 – Posology and Method of Administration |
Change in position of ‘Children (under 6 years of age) section to beginning of section 4.2. |
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Change to section 4.4 – Special Warnings and Precautions for Use |
Change in position of ‘Use in patients with renal hepatic impairment’ from this section into section 4.2 Under section heading ‘Galactose intolreance’ additional statement adding ‘This medicinal product contains lactose’ |
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Change to section 4.5 –Interaction with other medicinal products and other forms of interaction |
Addition of cross-references to sections 4.3 and 4.4 |
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Change to section 4.6 – Pregnancy and Lactation |
Addition of section headings: ‘Women of childbearing potential/Contraception ; Pregnancy ; Lactation |
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Change to section 6.1 – List of Excipients |
Excipients capitalised and listed sequentially |
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Change to section 6.6 – Instructions for use, handling and disposal |
Section heading updated |
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Change to section 9 – Date of Renewal of Authorisation |
Updated to add ‘6 June 2007’ ; sub-section headings added |
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Change to section 10 – Date of revision of the text |
Updated to add ‘6 June 2007’ |
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Change to joint SPC covering all presentations |
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Updated on 08 March 2007
Reasons for updating
- Correction of spelling/typing errors
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 16 January 2007
Reasons for updating
- Change to warnings or special precautions for use
- Change of contraindications
Updated on 11 January 2007
Reasons for updating
- 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
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
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Change to section 4.4 – Special Warnings and Precautions for Use |
Updated: warning in patients with cardiac structural abnormalities |
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Change to section 4.5 –Interaction with other medicinal products and other forms of interaction |
Updated INN names for Phenobarbital and amfetamine |
Updated on 19 May 2005
Reasons for updating
- Change to storage instructions
- Change to warnings or special precautions for use
Updated on 17 May 2005
Reasons for updating
- Change to section 4.4 - Special warnings and precautions for use
- Change to section 6.5 - Nature and contents of container
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 16 November 2004
Reasons for updating
- New PIL for medicines.ie
Updated on 18 March 2004
Reasons for updating
- Change to section 10 - Date of revision of the text
- Change to section 4.8 - Undesirable effects
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 05 June 2003
Reasons for updating
- New SPC for medicines.ie
Legal category:Product subject to medical prescription which may not be renewed (A)