Alverine Citrate 60 Mg Hard Capsules
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Alverine citrate 60 mg hard capsules
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each capsule contains 60 mg of alverine citrate.
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Hard capsules.
The hard gelatine capsules are white and oblong (size 3).
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
The relief of smooth muscle spasm, in conditions such as irritable bowel syndrome, painful diverticular disease of the colon and primary dysmenorrhoea.
4.2 Posology and method of administration
Recommended dose and dosage schedules:
Adults (including the elderly): 1 or 2 capsules one to three times daily.
Children below the age of 12 years: not recommended.
4.3 Contraindications
- Paralytic ileus
- Known hypersensitivity to any of the ingredients
- Intestinal obstruction.
4.4 Special warnings and precautions for use
Additional warnings to be included in the Patient Information Leaflet:
If this is the first time you have had these symptoms, consult your doctor before using any treatment.
If any of the following apply do not use this medicinal product; it may not be the right treatment for you. See your doctor as soon as possible if:
- you are aged 40 years or over
- you have passed blood from the bowel
- you are feeling sick or vomiting
- you have lost your appetite or lost weight
- you are looking pale and feeling tired
- you are suffering from severe constipation
- you have a fever
- you have recently travelled abroad
- you are or may be pregnant
- you have abnormal vaginal bleeding or discharge
- you have difficulty or pain passing urine.
Consult your doctor if you have developed new symptoms, or if your symptoms worsen, or if they do not improve after 2 weeks treatment.
4.5 Interaction with other medicinal products and other forms of interaction
Not stated.
4.6 Fertility, Pregnancy and lactation
Although no teratogenic effects have been reported, use during pregnancy or lactation is not recommended as evidence of safety in preclinical studies is limited.
4.7 Effects on ability to drive and use machines
May cause dizziness. Do not drive or use machinery if affected.
4.8 Undesirable effects
Immune system disorders: Allergic reaction, anaphylaxis, dyspnoea and/or wheezing
Nervous system disorders: Headache, dizziness Gastrointestinal disorders: Nausea
Hepato-biliary disorders: Jaundice due to hepatitis, typically this resolves on cessation of alverine
Skin and subcutaneous tissue disorders: Itching, rash Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.
4.9 Overdose
Can produce hypotension and atropine-like toxic effects. Management is as for atropine poisoning with supportive therapy for hypotension.
Fatality has occurred following overdose with very high doses.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Other drugs for functional bowel disorders, ATC code: A03AX08
Alverine citrate is a spasmolytic, which has a specific action on the smooth muscle of the alimentary tract and uterus, without affecting the heart, blood vessels and tracheal muscle at therapeutic doses.
5.2 Pharmacokinetic properties
After oral administration, alverine is rapidly converted to its primary active metabolite, which is then further converted to two secondary metabolites. There is a high renal clearance of all metabolites indicating that they are eliminated by active renal secretion. The peak plasma level of the most active metabolite occurs between 1 and 1% hours after oral dosing.
The plasma half-life averages 0.8 hours for alverine and 5.7 hours for the active primary metabolite.
5.3 Preclinical safety data
Although preclinical data are limited, those available indicate that alverine citrate has no significant potential for toxicity at the proposed dose level
Alverine citrate acts selectively on gut and uterine muscle, only affecting the heart, blood vessels and tracheal muscle at considerably higher doses.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Starch (maize) pregelatinised Magnesium stearate (E572)
Capsule shell Gelatin
Titanium dioxide (E171)
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
3 years.
6.4 Special precautions for storage
This medicinal product does not require any special storage conditions.
6.5 Nature and contents of container
Blister packs consisting of PVC/Aluminium.
Pack sizes of 3, 10, 12, 20, 30, 60, 90 or 100 white hard capsules.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal
No special requirements.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
7 MARKETING AUTHORISATION HOLDER
Dr. Reddy’s Laboratories (UK) Ltd.
6 Riverview Road Beverley East Yorkshire HU17 OLD United Kingdom
8 MARKETING AUTHORISATION NUMBER(S)
PL 08553/0532
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
03/06/2014
10 DATE OF REVISION OF THE TEXT
29/09/2014