Methotrexate Oral Solution
Methotrexate is an immunosuppressant.
Methotrexate Oral Solution is indicated for:
The maintenance treatment of Acute Lymphocytic Leukaemia (ALL) in children and adults.
The treatment of malignant trophoblastic tumours
The treatment of severe active rheumatoid arthritis in adults.
Polyarthritic forms of active, severe juvenile idiopathic arthritis (JIA) in adolescents and children aged 3 years and over when the response to non-steroidal anti-inflammatory drugs (NSAIDs) has been inadequate.
The treatment of severe forms of psoriasis vulgaris including chronic plaque psoriasis, erythrodermic psoriasis, psoriatic arthritis and pustular psoriasis which are not responsive to other conventional therapies such as phototherapy, PUVA and retinoids.
Summary of Product Characteristics
Read this summary of product characteristics for further information about Methotrexate Oral Solution. Click below to navigate to the EMC.
Patient Information Leaflet
Read this patient information leaflet about Methotrexate Oral Solution, what it’s used for and possible side effects. Click below to navigate to the EMC.
Methotrexate Oral Solution
Click here for Audio Version | |
Flavour | Raspberry |
Storage Conditions | Do not store above 25°C. Do not refrigerate. Store in original carton to protect from light. |
Sucrose Free | |
Shelf Life (Closed Bottle/Open Bottle) | 18 months / 3 months |
PIP Code | 120-5053 |
EAN Code | 05016119000416 |
Sodium Levels | Essentially sodium-free |
Ethanol Concentration | None |
Downloads
Click here for Audio Version | |
Flavour | Raspberry |
Storage Conditions | Do not store above 25°C. Do not refrigerate. Store in original carton to protect from light. |
Sucrose Free | |
Shelf Life (Closed Bottle/Open Bottle) | 18 months / 3 months |
PIP Code | 120-5046 |
EAN Code | 05016119000423 |
Sodium Levels | Essentially sodium-free |
Ethanol Concentration | None |
Downloads
Adverse Events
Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk
Adverse events should also be reported to Rosemont at 0113 244 1400 or pharmacovigilance@rosemontpharma.com.
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