Megacal-M Solution for Injection
Calcium, Magnesium
Last verified
Veterinary medicinal product: solution for injection. Distribution category: POM-VPS (Veterinary Medicines Regulations 2013, Schedule 3). Active substance: Calcium, Magnesium.1
In short: questions and answers
- Does Megacal-M Solution for Injection need a prescription?
- Status not established. Neither the leaflet nor the law settles how this drug is dispensed, and we do not guess.
- Which animals is Megacal-M Solution for Injection for?
- Cattle.1
- What is the active substance in Megacal-M Solution for Injection?
- Calcium, Magnesium.1
- What is the withdrawal period of Megacal-M Solution for Injection according to the leaflet?
- Cattle, meat: 0 days; Cattle, milk: 0 days.3
- Dispensing
- Status not established
POM-VPS: Prescription Only Medicine - Veterinarian, Pharmacist, Suitably Qualified Person. Prescription only, but the prescription may come from a veterinary surgeon, a pharmacist or a suitably qualified person (SQP, a registered animal-medicine adviser), and they may supply it.12
- Animal species
- Cattle1
- Active substance
- Calcium, Magnesium
- Manufacturer
- Marketing authorisation holder: Ballinskelligs Veterinary Products
Withdrawal period
Summary of product characteristics
Composition
Active Substance:
| Calcium (as Calcium Gluconate) | 4.6g/100ml |
|---|---|
| Magnesium (as Magnesium Hypophosphite) | 0.8g/100ml |
Excipient:
Boric Acid 10.0g/100ml
For the full list of excipients, see section 6.1
6.1 List of Excipients
Boric Acid
Water for Injection
Sodium Hydroxide (For pH adjustment)
Acetic Acid (For pH adjustment)
Pharmaceutical form
Solution for injection A colourless to pale yellow solution
Pharmacological properties
This product is intended to restore blood calcium levels in cases of hypocalcaemia.
Target species
Cattle
Indications
For treatment of hypocalcaemia and as an aid in raising blood magnesium levels where a deficiency may be expected.
Dosage
By subcutaneous or slow intravenous injection.
Cattle – 100 - 200ml.
Large volumes should be divided between multiple sites. Massage sites gently.
Contraindications
Known hypersensitivity to the to the active ingredients.
Known cases of cardiac arrhythmia or severe toxaemia
Adverse reactions
None known
Warnings
Warm the product to body temperature before administration. When the intravenous route is being used, extreme caution must be taken to ensure slow administration.
This product does not contain an antimicrobial preservative. Any solution remaining in the vial after withdrawal of the required dose should be discarded.
Special precautions to be taken by the person administering the product to animals
Care should be taken to avoid accidental self-injection. If accidental self-injection occurs, seek medical advice.
Eye Contact: immediately flush the eye with copious amounts of clean running water.
Skin contact: Wash the affected area thoroughly. If irritation occurs seek medical advice.
Ingestion: If accidentally swallowed, seek urgent medical attention and show product label and / or pack insert to the doctor.
ADVICE TO DOCTOR: For treatment advice contact the National Poisons Information Service (NPIS) or your local Poisons Information Centre.
Use during pregnancy, lactation or lay
Safe for use during pregnancy and lactation
Interactions
None known.
Overdose
The product is for treatment of acute deficiency in a life threatening situation and overdosage within the recommended guidelines is unlikely.
Special warnings
The product should be administered with care particularly where concurrent toxaemia exists. In recumbent cows with poor peripheral circulation, administer appropriate calcium therapy intravenously.
Withdrawal period
Meat – Zero days Milk – Zero hours
Incompatibilities
None known
Immediate packaging
A 100ml clear glass vial with nitryl rubber bung and gold seal containing a clear, colourless to pale yellow sterile solution
Storage
Store below 25°C. Protect from light.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 3 years.
Disposal of unused product
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed if in accordance with local requirements.
Additional information
Vm 12828/4000
9 DATE OF FIRST AUTHORISATION
01 February 1999
10 DATE OF REVISION OF THE TEXT
January 2015
Registration holder
Ballinskelligs Veterinary Products,
Ballinskelligs,
Co. Kerry,
Ireland.
Regulations
- Veterinary Medicines Regulations 2013 (SI 2013/2033), Schedule 32