Drugs Index
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Drug Classes
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Drugs Information:
Drugs List
1. Name Of The Medicinal Product
Galpharm Non-Drowsy Hayfever & Allergy Relief
Asda Non- Drowsy Hayfever & Allergy Relief
Tesco Non-Drowsy Hayfever & Allergy Relief
Morrison's Non-Drowsy Hayfever & Allergy Relief
Boots Non-Drowsy Hayfever Relief 10 mg Tablets
Value Health Non-Drowsy Hayfever & Allergy Relief
Sainsbury's Non-Drowsy Hayfever & Allergy Relief
Superdrug Non-Drowsy Hayfever & Allergy Relief
Numark Non-Drowsy Hayfever & Allergy Relief
Wilkinson's Non-Drowsy Hayfever & Allergy Relief
2. Qualitative And Quantitative Composition
Each tablet contains 10 mg of loratadine.
For excipients, see 6.1.
3. Pharmaceutical Form
Tablet
White, oval tablets, scored on one side and plain on the other side, debossed “L” and “10” on each side of the scoreline.
4. Clinical Particulars
4.1 Therapeutic Indications
Galpharm Non-Drowsy Hayfever & Allergy Relief tablets are indicated for the symptomatic treatment of allergic rhinitis and chronic idiopathic urticaria.
4.2 Posology And Method Of Administration
Adults and children 12 years of age and over: 10mg daily (one tablet once daily).
The tablets may be taken without regard to mealtime.
Children aged 2 to under 12 years with:
Body weight more than 30 kg: 10mg daily (one tablet once daily).
Body weight 30 kg or less: The 10mg strength tablet is not appropriate in children with a body weight less than 30 kg.
Efficacy and safety of Galpharm Non-Drowsy Hayfever & Aller
1. Name Of The Medicinal Product
Fenbid Forte 10% Gel
AAH Pharmaceutical's Ibuprofen pain relief gel maximum strength 10% w/w
Tesco's Ibuprofen pain relief gel maximum strength 10% w/w
Boots Ibuprofen 10% gel
Lloydspharmacy's Maximum strength Ibuprofen 10% gel
Ibuprofen 10% gel
Numark's Ibuprofen Pain Relief Gel Maximum Strength 10% w/w
Morrison's Ibuprofen Pain Relief Gel Maximum Strength 10% w/w
Thornton &Ross's Ibuprofen 10% gel
Phorpain gel maximum strength
Boots Ibuprofen Max Strength 10% Gel
2. Qualitative And Quantitative Composition
Ibuprofen Ph. Eur. 10% Gel
3. Pharmaceutical Form
Gel for topical application
4. Clinical Particulars
4.1 Therapeutic Indications
Prescription Only indication
For the relief of pain and inflammation associated with backache, mild to moderate arthritic conditions, rheumatic and muscular pain, sprains, strains, sports injuries and neuralgia.
Pharmacy Only indication
For the relief of pain and inflammation associated with backache, rheumatic and muscular pain, strains, sprains, neuralgia and sports injuries. For the relief of pain of non-serious arthritic conditions.
4.2 Posology And Method Of Administration
Method of administration
For topical application to the skin.
Dosage
Adults, the elderly and children over 14 years: Squeeze 50 to 125mg (2 to 5cm) of the gel from the tube and lightly rub into the affected area until absorbed.
1. Name Of The Medicinal Product
BurnEze Spray.
2. Qualitative And Quantitative Composition
Benzocaine Ph Eur 1.0% w/w.
3. Pharmaceutical Form
Aerosol spray.
4. Clinical Particulars
4.1 Therapeutic Indications
For the symptomatic relief of pain from minor superficial burns and scalds where the skin is unbroken.
4.2 Posology And Method Of Administration
For topical administration. Adults, the elderly, and children: To reduce pain and blistering, use BurnEze Spray as quickly as possible. Hold nozzle five inches from the skin and spray once for 2-3 seconds. Stop spraying immediately if a white frost deposit (frost) appears. If necessary, the application may be repeated once only after 15 minutes. If pain persists seek medical advice.
4.3 Contraindications
Do not use if you are sensitive to benzocaine.
4.4 Special Warnings And Precautions For Use
Patients with any known allergy should seek medical advice. Do not apply to large areas or to broken skin. Do not use in or near the mouth or eyes or under conditions in which significant inhalation is likely. Avoid freezing the skin by repeated or prolonged use. Seek medical advice immediately if burns are extensive (particularly in young children or if they affect fingers, toes or sensitive areas). For external use only. Keep out of the reach of children. Flammable. Do not use near fire or flame. Pressurised container. Protect from sunlight and do not expose to temperatures exceeding 50oC. Do not pierce or burn, even after use. Do not spray on a naked flame or any incandescent material. Do not use near or place container on polished or painted surfaces.
4.5 Interaction With Other Medicinal Products And Other
1. Name Of The Medicinal Product
Brevinor.
2. Qualitative And Quantitative Composition
Each tablet contains 0.5 milligrams norethisterone and 35 micrograms ethinylestradiol.
3. Pharmaceutical Form
Blue, flat, circular, bevel-edged tablet inscribed 'SEARLE' on one side and 'BX' on the other side.
4. Clinical Particulars
4.1 Therapeutic Indications
Brevinor is indicated for oral contraception, with the benefit of a low intake of oestrogen.
4.2 Posology And Method Of Administration
Oral Administration: The dosage of Brevinor for the initial cycle of therapy is 1 tablet taken at the same time each day from the first day of the menstrual cycle. For subsequent cycles, no tablets are taken for 7 days, then a new course is started of 1 tablet daily for the next 21 days. This sequence of 21 days on treatment, seven days off treatment is repeated for as long as contraception is required.
Patients unable to start taking Brevinor tablets on the first day of the menstrual cycle may start treatment on any day up to and including the 5th day of the menstrual cycle.
Patients starting on day 1 of their period will be protected at once. Those patients delaying therapy up to day 5 may not be protected immediately and it is recommended that another method of contraception is used for the first 7 days of tablet-taking. Suitable methods are condoms, caps plus spermicides and intra-uterine devices. The rhythm, temperature and cervical-mucus methods should not be relied upon.
Tablet omissions
Tablets must be taken daily in order to maintain adequate hormone levels and contraceptive efficacy.
If a tablet is missed within 12 hours of the correct dosage ti
Boots Easy Breathing Pastilles
(Abietis Oil, Menthol, Sylvestris Pine Oil)
Relieves congestion due to coughs and catarrh
45 g e
Read all of this carton for full instructions.
Uses: This medicine contains a combination of decongestant oils for the relief of the symptoms of catarrh and coughs.
Before you take this medicine
Do not take:
- If you are allergic to any of the ingredients
- If you have an intolerance to some sugars, unless your doctor tells you to (this medicine contains glucose and sucrose)
Talk to your pharmacist or doctor:
- If you are pregnant or breastfeeding
Information about some of the ingredients: Each pastille contains a total of 1.3 g of glucose and sucrose. This should be taken into account by people with diabetes.
How to take this medicine
Check the inner bag is not broken before use. If it is, do not use the pastilles.
Adults and children of 12 years and over: Suck one pastille, when you need to.
Don’t take more than 18 pastilles in 24 hours.
Children of 6 to 11 years: Suck one pastille, when you need to. Don’t take more than 12 pastilles in 24 hours.
Suck each pastille slowly until it dissolves.
Do not give to children under 6 years.
Do not take more than the amou
1. Name Of The Medicinal Product
After Bite
Boots Bite & Sting Relief Liquid
2. Qualitative And Quantitative Composition
After Bite contains Strong Ammonia Solution BP corresponding to 3.5% w/v ammonia.
3. Pharmaceutical Form
Topical emulsion for cutaneous application.
4. Clinical Particulars
4.1 Therapeutic Indications
Relief from insect bites, including mosquitoes, horse flies, and relief from stings including wasps, bees, jellyfish and nettles.
4.2 Posology And Method Of Administration
Cutaneous administration.
For adults and children over 2 years old
Apply as required. Rub applicator on affected area. Prompt use gives maximum relief. If itching persists repeat the application. Do not bandage or cover tightly until dry.
Daub the After Bite directly on the bite or sting. Apply promptly to the bite for best results. If itching persists or recurs, repeat application. Replace cap after each use.
4.3 Contraindications
After Bite is contraindicated in individuals with known hypersensitivity to ammonia.
4.4 Special Warnings And Precautions For Use
Keep out of reach of children. For external use only. If swallowed do not induce vomiting. Drink milk and citrus juices and consult a doctor.
If rash, redness, irritation, swelling or pain increases or worsen after application, discontinue use and seek medical advice.
Avoid mouth or eyes. If this should occur rinse well with water.
The insect bite should be left exposed to the air for a brief period of time after application to aid in evaporation of ammonia.
The label shall
Boots Pharmacy Thrush Duo
(Clotrimazole, Fluconazole)
Read all of this leaflet carefully because it contains important information for you.
This medicine is available without prescription to treat minor conditions. However, you still need to take it carefully to get the best results from it.
- Keep this leaflet, you may need to read it again
- Ask your pharmacist if you need more information or advice
What this medicine is for
This pack contains a cream and a single capsule. The cream contains Clotrimazole and the capsule contains Fluconazole. Both of these medicines belong to a group called anti-fungals, which act to treat infections caused by fungi.
The medicine can be used to treat thrush (vaginal candidiasis) and the external symptoms of thrush (vulval candidiasis). It may also be used by the woman’s sexual partner to treat associated penile thrush (candidal balanitis). The capsule can be taken by both men and women, the cream can be used by both partners too. If a woman and her partner both intend to take the capsule you will need one pack each.
Thrush is a common infection caused by a yeast (or fungus), which may live harmlessly in the vagina without you even noticing it. However, in certain circumstances, it may develop into an infection in the vagina and symptoms may spread to the surrounding area. The symptoms may include one or more of the following:
- Itching of the vagina and surrounding area (the vulva)
- Redness and swelling of the tissues of the vagina and vulva
- Soreness of the vagina and vulva
- A white non-smelling discharge from the vagina
Thrush may be aggravated by sexua
1. Name Of The Medicinal Product
BUFYL 1.25mg/ml and 2microgram/ml Solution for Infusion
2. Qualitative And Quantitative Composition
Each 1ml of solution contains 1.25mg bupivacaine hydrochloride and 2 micrograms fentanyl (as fentanyl citrate)
Also contains up to 3.5mg sodium per ml.
For a full list of excipients, see section 6.1.
3. Pharmaceutical Form
Solution for epidural infusion.
Clear, colourless aqueous sterile solution.
4. Clinical Particulars
4.1 Therapeutic Indications
Bufyl solution for infusion is indicated for:
(i) maintaining analgesia post-operatively and
(ii) for maintaining epidural analgesia during labour.
4.2 Posology And Method Of Administration
Route of administration: Epidural Infusion
Bufyl solution for infusion should only be administered epidurally and should only be used by, or under the supervision of, clinicians experienced in regional anaesthesia.
The dose administered must be tailored to the individual patient and procedure. When calculating the dosage for post-operative analgesia, the use of intra-operative bupivacaine and/or fentanyl (or other opioid agonist analgesic) should be taken into account. The rapid injection of bupivacaine with fentanyl solution should be avoided and the maximum accumulated dosage should not exceed 400 mg of bupivacaine and 720 microgram of fentanyl for a 24 hour period in a 70 kg adult.
Note: This formulation is not to be used as a bolus.
Adults:
The length of continuous epidural infusions given post-operatively should be minimized, due to the increased risks of r
Boots Allergy Relief Antihistamine Tablets
(Chlorphenamine Maleate)
Read all of this leaflet carefully because it contains important information for you.
This medicine is available without prescription to treat minor conditions. However, you still need to take it carefully to get the best results from it.
- Keep this leaflet, you may need to read it again
- Ask your pharmacist if you need more information or advice
What this medicine is for
This medicine contains Chlorphenamine Maleate which belongs to a group of medicines called antihistamines, which act to relieve the symptoms of allergies.
It can be used to relieve the symptoms of allergic reactions including hayfever, raised, red itchy skin (symptoms of urticaria, which is often known as hives or nettle rash), allergic reactions to foods or medicines, insect bites, runny nose and swelling of the face or throat due to fluid build up.
Before you take this medicine
This medicine can be taken by adults and children aged 1 year and over. However, some people should not take this medicine or should seek the advice of their pharmacist or doctor first.
Do not take:
- If you are allergic to any of the ingredients, or any other antihistamines
- If you are taking monoamine oxidase inhibitors (for depression) or have taken them within the last 14 days
- If you have an intolerance to some sugars, unless your doctor tells you to (this medicine contains lactose)
1. Name Of The Medicinal Product
Asda Max Strength Sinus Relief Capsules, Hard
Boots Max Strength Sinus Relief Capsules, Hard
Superdrug Max Strength Sinus Relief Capsules, Hard
Wilko Max Strength Sinus Relief Capsules, Hard
Non-Drowsy Sudafed Congestion and Headache Capsules, Hard
Sudafed Blocked Nose & Sinus Capsules
2. Qualitative And Quantitative Composition
| Active Ingredient | mg/Capsule |
| Paracetamol | 500 |
| Caffeine | 25 |
| Phenylephrine Hydrochloride | 6.1 |
For a full list of excipients, see section 6.1
3. Pharmaceutical Form
Capsule, hard.
Red/blue hard gelatin capsules containing the drug product, an off-white powder.
4. Clinical Particulars
4.1 Therapeutic Indications
For the relief of symptoms associated with the pain and congestion of sinusitis, including relief of aches and pains, headache, nasal congestion and lowering of temperature.
4.2 Posology And Method Of Administration
For oral use.
Swallow whole with water. Do not chew.
1. Name Of The Medicinal Product
Betoptic 0.5% w/v eye drops, solution
2. Qualitative And Quantitative Composition
Betaxolol 0.5% w/v (as hydrochloride)
3. Pharmaceutical Form
Eye Drops, Solution
4. Clinical Particulars
4.1 Therapeutic Indications
Betoptic is indicated for the reduction of elevated intraocular pressure in patients with ocular hypertension and chronic open angle glaucoma.
4.2 Posology And Method Of Administration
Adults (including the elderly)
The usual dose is one drop to be instilled into the affected eye(s) twice daily.
Children
Betoptic is not recommended for use in children.
4.3 Contraindications
Betoptic is contraindicated in patients with sinus bradycardia greater than a first degree block, cardiogenic shock or a history of overt cardiac failure and in patients with hypersensitivity to any component.
4.4 Special Warnings And Precautions For Use
Patients who are receiving a beta-adrenergic blocking agent orally and Betoptic should be observed for potential additive effect either on intraocular pressure or the known systemic effects of beta-blockade.
While Betoptic has demonstrated a low potential for systemic effects, it should be used with caution in patients with diabetes (especially labile diabetes) or in patients suspected of developing thyrotoxicosis.
Consideration should be given to the gradual withdrawal of beta-adrenergic blocking agents prior to general anaesthesia because of the reduced ability of the heart to respond to beta-adrenergically mediated sympathetic reflex stimuli.
1. Name Of The Medicinal Product
Mac Dual Action Honey Lemon Sore Throat Lozenges
Mac Dual Action Honey Lemon Flavour
Superdrug Honey & Lemon Sore Throat Dual Action Lozenges
Safeway Medicated Lozenges Honey & Lemon Flavour
Safeway Dual Action Lozenges Honey & Lemon Flavour
Benylin Sore Throat Honey & Lemon Lozenges.
Morrisons Dual Action Antiseptic Lozenges Honey & Lemon
Boots Sore Throat Relief Dual Action Lozenges Honey and Lemon Flavour
2. Qualitative And Quantitative Composition
Hexylresorcinol 2.4 mg per lozenge
3. Pharmaceutical Form
Lozenge
4. Clinical Particulars
4.1 Therapeutic Indications
As an antiseptic, demulcent and local anaesthetic for the relief of sore throat and its associated pain.
4.2 Posology And Method Of Administration
For adults and children aged 6 years and over:-
One lozenge dissolved slowly in the mouth every 3 hours or as required
Do not take more than 12 lozenges in 24 hours.
For the elderly:-
The normal adult dosage may be taken
4.3 Contraindications
Hypersensitivity to any of the ingredients
4.4 Special Warnings And Precautions For Use
Labelling: Keep out of reach of children. If symptoms persist consult your doctor. Not to be given to children under 6 years.
Do not take if you suffer from fructose intolerance or a related metabolic disorder.
4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction
None known.
4.6 Pregnancy And Lactation
1. Name Of The Medicinal Product
BYDUREON®
2. Qualitative And Quantitative Composition
Each vial contains 2 mg of exenatide.
For a full list of excipients, see section 6.1.
3. Pharmaceutical Form
Powder and solvent for prolonged-release suspension for injection.
Powder: white to off-white powder.
Solvent: clear, colourless to pale yellow to pale brown solution.
4. Clinical Particulars
4.1 Therapeutic Indications
BYDUREON is indicated for treatment of type 2 diabetes mellitus in combination with
• Metformin
• Sulphonylurea
• Thiazolidinedione
• Metformin and sulphonylurea
• Metformin and thiazolidinedione
in adults who have not achieved adequate glycaemic control on maximally tolerated doses of these oral therapies.
4.2 Posology And Method Of Administration
Posology
The recommended dose is 2 mg exenatide once weekly.
Patients switching from exenatide twice daily (BYETTA) to BYDUREON may experience transient elevations in blood glucose concentrations, which generally improve within the first two weeks after initiation of therapy.
When BYDUREON is added to existing metformin and/or thiazolidinedione therapy, the current dose of metformin and/or thiazolidinedione can be continued. When BYDUREON is added to sulphonylurea therapy, a reduction in the dose of sulphonylurea should be considered to reduce the risk of hypoglycaemia (see section 4.4).
BYDUREON should be administered once a week on the same day each week. The day of weekly administration can be changed if necessary as long as the next
1. Name Of The Medicinal Product
Bisacodyl Tablets 5mg
2. Qualitative And Quantitative Composition
Each tablet contains bisacodyl BP 5mg
3. Pharmaceutical Form
Enteric coated tablet
4. Clinical Particulars
4.1 Therapeutic Indications
For short-term use for constipation, whenever a stimulant laxative is required.
Bowel clearance before surgery, labour or radiological examination, all of which should be under medical supervision.
4.2 Posology And Method Of Administration
In constipation:
Adults and children over 10 years old: 2 tablets (10mg) at night; occasionally a higher dosage is required, and up to 3 or 4 tablets (15mg to 20mg) may be given.
Elderly: As for adults. It may be necessary to reduce the dosage under certain circumstances.
Children 3 to 10 years old: 1 tablet (5mg) at night.
Children under 3 years old: Not recommended.
Before surgery, labour or hospital radiological examination:
Adults and children over 10 years old: 2 tablets (10mg) on each of 2 nights before the anticipated procedure.
Elderly: As for adults. It may be necessary to reduce the dosage under certain circumstances.
Children 3 to 10 years old: 1 tablet (5mg) on each of 2 nights before the investigation.
Children under 3 years old: Not recommended.
Method of administration: oral.
4.3 Contraindications
Intestinal obstruction, ileus and those where a contact laxative is contra-indicated.
4.4 Spec
Boots Skin Therapy Emollient Cream
(Almond Oil, Lanolin)
Effective relief for dry skin conditions
Soothes
Moisturisers
Relieves
relieves dry skin conditions such as dry eczema, chapping, nappy soreness and sunburn
300 g e
Read all of this label for full instructions.
What this medicine is for
An emollient cream that relieves dry skin conditions such as dry eczema, chapping, nappy soreness and sunburn.
Before you use this medicine
X Do not use:
- If you are allergic to any of the ingredients
You can use this medicine if you are pregnant or breastfeeding.
Cetyl alcohol may cause skin reactions (e.g. contact dermatitis).
How to use this medicine
Check the tub seal is not broken before first use. If it is, do not use the cream. To open, lift tear strip and pull around tub.
Apply to the skin only.
Adults and children: Use on the affected area 2 or 3 times a day.
If symptoms do not go away talk to your pharmacist or doctor.
If anyone accidentally swallows some: Talk to a pharmacist or doctor.
Possible side effects
Most people will not have problems.
If you get these side effects stop using the cream and see a doctor:
- Allergic reaction (e.g. skin rash, red or itchy skin)
If you notice any side effect not listed here, please tell your pharma
1. Name Of The Medicinal Product
Becodisks 200 Micrograms
2. Qualitative And Quantitative Composition
Beclometasone Dipropionate 200micrograms
3. Pharmaceutical Form
Dry Powder for Inhalation via Diskhaler Device
4. Clinical Particulars
4.1 Therapeutic Indications
Clinical Indications
Beclometasone dipropionate provides effective anti-inflammatory action in the lungs, with a lower incidence and severity of adverse effects than those observed when corticosteroids are administered systemically. It also offers preventive treatment of asthma.
Becodisks are indicated for the following:
Adults
Prophylactic management in:
Mild asthma (PEF values greater than 80% predicted at baseline with less than 20% variability):
Patients requiring intermittent symptomatic bronchodilator asthma medication on more than an occasional basis.
Moderate asthma (PEF values 60-80% predicted at baseline with 20-30% variability):
Patients requiring regular asthma medication and patients with unstable or worsening asthma on other prophylactic therapy or bronchodilator alone.
Severe asthma (PEF values less than 60% predicted at baseline with greater than 30% variability):
Patients with severe chronic asthma. On transfer to high dose inhaled beclometasone dipropionate, many patients who are dependent on systemic corticosteroids for adequate control of symptoms may be able to reduce significantly or eliminate their requirement for oral corticosteroids.
4.2 Posology And Method Of Administration
Becodisks are for administration by the inhalation ro
1. Name Of The Medicinal Product
Ibuprofen 5% gel,
Fenbid gel,
Phorpain Gel
Flexigel,
Boots Ibuprofen Gel, Ibuprofen Pain Relief Gel
Nurofen 5% gel,
Morrison's Ibuprofen pain relief 5% w/w gel
Ibucalm Ibuprofen Pain Relief Gel 5 % w/w
Ibuprofen Pain relief gel 5% w/w
Bell's Healthcare Ibuprofen 5% gel
Sainsbury's Ibuprofen 5% w/w gel
2. Qualitative And Quantitative Composition
5% w/w Ibuprofen Ph.Eur.
3. Pharmaceutical Form
Gel for topical application.
4. Clinical Particulars
4.1 Therapeutic Indications
Pharmacy Only Indications:
Topical analgesic and anti-inflammatory for backache, pain of non-serious arthritic conditions, muscular pain, sprains, strains, sports injuries and neuralgia.
General Sales List Indications:
Topical analgesic and anti-inflammatory for backache, rheumatic and muscular pain, sprains, strains and sports injuries.
4.2 Posology And Method Of Administration
Strength 5% maximum
Method of Administration
For topical application to the skin.
Dosage
Adults, the elderly and children over 14 years: Squeeze 50 to 125mg (4 to 10cm) of the gel from the tube and lightly rub into the affected area until absorbed. The dose should not be repeated more frequently than every four hours and no more than 4 times in any 24 hour period. Wash hands after each application. Do not exceed the stated dose. Review treatment after 2 weeks, especially if the symptoms worsen or persist.
1. Name Of The Medicinal Product
Balneum Plus
2. Qualitative And Quantitative Composition
|
Active ingredients: |
%w/w |
|
Soya oil |
82.95 |
|
Lauromacrogols |
15.00 |
3. Pharmaceutical Form
Bath oil
4. Clinical Particulars
4.1 Therapeutic Indications
Balneum Plus is a bath oil the active ingredients of which have emollient and local anaesthetic properties and provide relief of pruritus. It is recommended for the treatment of dry skin conditions including those associated with dermatitis and eczema where severe pruritus is also experienced.
4.2 Posology And Method Of Administration
After shaking the bottle, Balneum Plus should be added to the bath water and mixed well.
Frequency and duration of the application should be adjusted according to the type and severity of the condition, adults should use the bath oil frequently (at least 3 times per week) whilst neonates and infants should be treated daily.
Dosage
The following quantities are recommended: (If the skin requires considerable moisturising, 2-3 times these quantities can be used)
Adults (including the elderl
1. Name Of The Medicinal Product
Acidex, Compound Alginate Oral Suspension, Heartburn and Indigestion Liquid
Compound Alginate, Oral Suspension, Heartburn and Indigestion Liquid
Brunel Healthcare Heartburn and Indigestion Liquid
Superdrug Acid Indigestion and Heartburn Relief Liquid
Heartburn and Indigestion Relief
SETLERS Heartburn and Indigestion Liquid
Coalgicarb Suspension
Lloydspharmacy Heartburn and Indigestion Liquid
Raft-Eze Liquid
Boots Heartburn Relief Aniseed Flavour
Co-op Heartburn and Indigestion Liquid
Entrocalm Heartburn and Indigestion Relief
Morrisons Heartburn and Indigestion Liquid
Peptac Liquid (Ivax Pharmaceuticals UK)
Asda Heartburn and Indigestion Liquid
Numark Heartburn and Indigestion Liquid
Wilkinson Heartburn and Indigestion Liquid
Sainsbury's Heartburn and Indigestion Liquid
2. Qualitative And Quantitative Composition
Each 5ml contains:
Sodium Bicarbonate BP - 133.5mg
Sodium Alginate BP - 250mg
Calcium Carbonate - 80mg
3. Pharmaceutical Form
Aniseed flavoured pink suspension.
4. Clinical Particulars
4.1 Therapeutic Indications
Acidex Compound Alginate Oral Suspension Heartburn and Indigestion Liquid alleviates the painful conditions resulting from the reflux of gastric acid and bile into the oesophagus by suppressing the reflux itself. It is indicated in heartburn, including heartburn of pregnancy, dyspepsia associated with gastric reflux, hiatus hernia, reflux oesophagitis, regurgitation and all cases of epigastric and r
1. Name Of The Medicinal Product
Decongestant Tablets
2. Qualitative And Quantitative Composition
|
Active ingredient |
|
|
Pseudoephedrine hydrochloride |
60mg/tablet |
3. Pharmaceutical Form
Tablets
4. Clinical Particulars
4.1 Therapeutic Indications
For the relief of nasal and sinus congestion without causing drowsiness.
For oral administration.
4.2 Posology And Method Of Administration
Adults and children over 12 years: One tablet if necessary, up to four times daily at intervals of not less than 4 hours.
Children under 12 years: Not recommended.
Elderly: There is no need for dosage reduction in the elderly.
4.3 Contraindications
Hypersensitivity to any of the ingredients. Avoid in patients with cardiovascular disease, hypertension, severe renal impairment, diabetes mellitus, closed angle glaucoma, hyperthyroidism, prostatic enlargement and phaeochromocytoma.
4.4 Special Warnings And Precautions For Use
If symptoms are not controlled by Boots Decongestant Tablets, medical advice should be sought.
Keep all medicines out of the reach of children.
Warning: Do not exceed the stated dose.