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AstraZeneca Pharmaceuticals (Ireland) Ltd

AstraZeneca Pharmaceuticals (Ireland) Ltd
College Park House, 20 Nassau Street, Dublin 2,
Telephone: +353 1 609 7100
Fax: +353 1 679 6650
Medical Information Direct Line: 1800 800 899 Freephone
Medical Information e-mail: medical.informationuk@astrazeneca.com
Customer Care direct line: +353(0)1 609 7100 Supply & non-medical enquiries
Medical Information Facsimile: +44 (0)1582 838 003
Summary of Product Characteristics last updated on medicines.ie: 17/08/2009
SPC NIFTEN

When a pharmaceutical company changes an SPC or PIL, 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 17/08/2009 and displayed until Current
Reasons for adding or updating:
  • Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
  • Change to section 6.1 - List of excipients
  • Change to section 10 - Date of revision of the text
Date of revision of text on the SPC:   31-Jul-2009
Legal Category:   Product subject to medical prescription which may be renewed (B)

Free-text change information supplied by the pharmaceutical company

Section 4.5
New third paragraph:
"Class I anti-arrhythmic drugs (eg, disopyramide) and amiodarone may have a potentiating effect on atrial-conduction time and induce negative inotropic effect."

Section 6.1
Reformatted list of excipients
"

Granule

Maize starch

Heavy magnesium carbonate

Sodium laurilsulfate

Gelatin

Magnesium stearate

 

Tablet core

Microcrystalline cellulose

Maize starch

Lactose monohydrate

Polysorbate 80

Magnesium stearate

 

Tablet coating

Hypromellose

Macrogol 4000

Titanium dioxide (E171)

Iron oxide red (E172)

 

Capsule shell

Iron oxide red (E172)

Titanium dioxide (E171)

Gelatin

 

Printing ink

Shellac

Soya lecithin

Titanium dioxide (E171)

2-ethoxyethanol

                Dimethylpolysiloxane"

Section 10
31st July 2009

Updated on 19/09/2008 and displayed until 17/08/2009
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
Date of revision of text on the SPC:   08/2008
Legal Category:   prescription only

Free-text change information supplied by the pharmaceutical company

Section 4.5

Change of text in 6th paragraph

Original text: Caution must be exercised when prescribing a beta-blocker with Class 1 antiarrhythmic agents such as disopyramide.

Changed to:

Class I anti-arrhythmic drugs (eg, disopyramide) and amiodarone may have a potentiating effect on atrial-conduction time and induce negative inotropic effect.

 

Section 10
Date of revision of text: 29 August 2008
Updated on 16/04/2007 and displayed until 19/09/2008
Reasons for adding or updating:
  • Change to section 2 - Qualitative and quantitative composition
  • Change to section 3 - Pharmaceutical form
  • 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
  • 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 4.9 - Overdose
  • Change to section 5.1 - Pharmacodynamic properties
  • Change to section 6.1 - List of excipients
  • Change to section 6.2 - Incompatibilities
  • Change to section 6.4 - Special precautions for storage
  • Change to section 6.5 - Nature and contents of container
  • 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
Date of revision of text on the SPC:   03/2006
Legal Category:   prescription only

Free-text change information supplied by the pharmaceutical company

Section 2

Text change:

Each capsule contains 50 mg atenolol and 20 mg nifedipine added and Atenolol 50mg , Nifedipine 20mg removed

Additional text added:

For excipients, see section 6.

 

Section 3

Additional text added:

Capsules, hard added

 

Section 4.2

Additional text added, last paragraph:

Renal Impairment

NIF-TEN should not be used in patients with marked renal impairment (see section 4.3).

 

Section 4.3

Additional text added(bold), first line in list:

Known hypersensitivity to either active component or any of the excipients.

 

Section 4.4

Additional text added (bold), second bullet point:

consequently the use of NIF-TEN may

 

Additional text added, ninth bullet point:

(epinephrine)

 

Section 4.5

Additional text added seventh paragraph:

(epinephrine)

 

Additional text added thirteenth paragraph:

Due to enzyme induction, rifampicin has been shown to decrease the nifedipine AUC and Cmax by 95% (288 ng.L/ml to 8 ng.L/ml and 154 ng/ml to 7.5 ng/ml respectively.  This may result in reduced efficacy, therefore co-administration of nifedipine with rifampicin is contraindicated (see section 4.3).

 

 

Section 4.8 

Additional text added(CNS):

dizziness, headache

Additional text added (Others)

fatigue

 

Section 4.9

Additional text added beginning of section:

Symptoms

The symptoms of overdosage may include bradycardia, hypotension, acute cardiac insufficiency and bronchospasm.

Treatment

General treatment should include: close supervision, treatment in an intensive care ward, the use of gastric lavage, activated charcoal as a laxative to prevent absorption of any drug still present in the gastrointestinal tract, the use of plasma or plasma substitutes to treat hypotension and shock. The possible use of haemodialysis or haemoperfusion may be considered.

 

Additional text added end of section:

or isoprenaline 10 to 25 micrograms given as an infusion at a rate not exceeding 5 micrograms/minute may be given, although larger doses may be required. Dobutamine, because of its positive inotropic effect could also be used to treat hypotension and acute cardiac insufficiency.  It is likely that these doses would be inadequate to reverse the cardiac effects of beta-blockade if a large overdose has been taken.  The dose of dobutamine should therefore be increased, if necessary, to achieve the required response according to the clinical condition of the patients.  In severe cases of hypotension, cardiac pacing with appropriate cardiac respiratory support may be necessary.  Bronchospasm can usually be reversed by bronchodilators.

 

 

Section 5.1

Additional text added beginning of section:

Beta-blocking agents and other antihypertensives

C07 FB

 

Section 6.1

Additional text added(bold):

Sodium laurilsulfate added and sodium Lauryl Sulphate removed

Lactose monohydrate

Hypromellose added and Methylhydroxypropylcellulose removed

 

Section 6.2

Text change:

None known changed to Not applicable

 

Section 6.4

Additional text added:

Store in the original package.  Keep the container in the outer carton.

 

Section 6.5

Foil/PVC removed and Additional text added:

PVC/PVDC/AL

 

Section 6.6

Text change:

None changed to No special requirements

 

Section 9

Additional text added:

29th September 2003

 

 

Section 10

Text change:

Previous dates removed new date added 31st march 2006

Updated on 15/08/2003 and displayed until 16/04/2007
Reasons for adding or updating:
  • New SPC for medicines.ie

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Active Ingredients

 
   Nifedipine
   Atenolol

Versions

 
17/08/2009 to Current
19/09/2008 to 17/08/2009
16/04/2007 to 19/09/2008
15/08/2003 to 16/04/2007
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Registered Address: Franklin House, 140 Pembroke Road, Dublin 4, Ireland
Registered Number: 254776
Tel: (353 1) 6603350 Fax: (353 1) 6686672 Email: info@ipha.ie

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