Recurring concern
Unreliable methotrexate safety information and guidance
First reported 16 Nov 2022•Latest report 20 Feb 2026
What this concern includes
Includes failures in the dedicated methotrexate safety-information and guidance process, including review of patient literature after adverse effects, current dosing guidance, toxicity warnings, treatment-continuation or cessation advice, and clear responsibilities and referral routes among clinicians and pharmacists.
Not included
- Excludes generic medication-guidance, patient-information or adverse-event-reporting deficiencies where methotrexate is not the material safety concern.
- Excludes failures in administering, dispensing or monitoring methotrexate after current and clear safety guidance has been provided.
- Excludes unrelated clinical conditions, medicines and treatment pathways without a direct methotrexate safety-information or guidance connection.
- Reports
- 2
- Individual concerns
- 4
- Date range
- 2022–2026
- Stated actions
- 3
Distinct published reports
A report can raise multiple concerns
First to latest report issue date
Described in published responses
Reports over time
Reports over time
Reports about this concern issued each year.
* 2026 is projected from reports observed to 7 Sep 2026.
Most frequent recipients
Most frequent recipients
Reports about this concern sent to each recipient.
Concerns and responses across reports
Only concerns grouped under this recurring concern are included. Select any concern, action or position to view the source wording.
-
Concerns raised2
Failure of the methotrexate guideline to provide a current therapeutic initial dose
Failure of the methotrexate guideline to define current responsibilities and direct patients to the appropriate healthcare professional
Responses linked to these concernsEach statement is shown once, even when linked to more than one concern.
Actions described in response An action is something a respondent says it has done, is doing, or plans to do in response to the concern raised.3
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Action
Continue making urgent safety amendments to shared care protocols through clinical governance processes.
Stated by NHS Greater Manchester Integrated Care Board -
Action
Review monitoring requirements and dosing wording in the shared care protocol against contemporary rheumatology guidance.
Stated by NHS Greater Manchester Integrated Care Board -
Action
Consider clarifying in the guideline who patients should contact when they develop concerning symptoms.
Stated by NHS Greater Manchester Integrated Care Board
Respondent positions A position is what a respondent says about the concern when they do not describe a specific action.3
-
Position
The methotrexate protocol’s dose range reflects current product information and guidance, with lower initial dosing supporting safety and specialist adjustment.
Stated by NHS Greater Manchester Integrated Care Board
-
Position
Patients with possible methotrexate toxicity should be assessed by their GP or specialist team, not community pharmacists.
Stated by NHS Greater Manchester Integrated Care Board -
Position
The patient was ineligible for Pharmacy First, so the service should not have managed the patient in this case.
Stated by NHS Greater Manchester Integrated Care Board
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Concerns raised2
Unclear criteria for reviewing patient literature after reports of methotrexate phototoxicity
Failure to include methotrexate phototoxicity in literature given to patients
Responses linked to these concernsEach statement is shown once, even when linked to more than one concern.
No linked response statementsNo respondent-stated action or position is linked to these concerns in the published data.
Data last updated 7 September 2026