Source: Health Products Regulatory Authority (IE) Revision Year: 2021 Publisher: Pfizer Healthcare Ireland, 9 Riverwalk, National Digital Park, Citywest Business Campus, Dublin 24, Ireland
Depo-Medrone 40mg/ml with Lidocaine 10mg/ml Suspension for Injection, 1ml vial.
Pharmaceutical Form |
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Suspension for Injection. Sterile white aqueous suspension. |
Each ml contains methylprednisolone acetate 40 mg and lidocaine hydrochloride 10 mg.
Each vial contains 40 mg methylprednisolone acetate and 10 mg lidocaine hydrochloride.
Excipient with known effect: Benzyl alcohol: 8.7 mg per ml.
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Lidocaine |
Lidocaine, like other local anaesthetics, causes a reversible blockade of impulse propagation along nerve fibres by preventing the inward movement of sodium ions through the nerve membrane. Local anaesthetics of the amide-type are thought to act within the sodium channels of the nerve membrane. |
|
Methylprednisolone |
Methylprednisolone is a synthetic glucocorticoid and a methyl derivative of prednisolone. Methylprednisolone is a potent anti-inflammatory agent with the capacity to profoundly inhibit the immune system. |
List of Excipients |
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Macrogol |
Type I flint glass vials with a butyl rubber cap. Each vial contains 1 ml of suspension.
Vials packed singly and in 10 vial packs.
Not all pack sizes may be marketed.
Pfizer Healthcare Ireland, 9 Riverwalk, National Digital Park, Citywest Business Campus, Dublin 24, Ireland
PA0822/123/001
Date of first authorisation: 05 July 1983
Date of last renewal: 28 January 2006
Drug | Countries | |
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DEPO-MEDRONE WITH LIDOCAINE | Ireland, United Kingdom, South Africa |
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