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Carers Concern Over Medication
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I am a carer for a man with severe ms who is home treated. His wife doses him with sativex, not prescribed.She gives him 6 squirts randomly & up to 4 times a day. A colleague refuses to give him more than 4 squirts as it makes him feel very unwell & he insists it has no affect on his spasms. I know little about sativex but my colleague insists that it should be administered over the course of 2 weeks & gradually built up for optimum affect is this correct & what can I do if it is not?
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Local authority carers where I live will not give medication at all unless the mes are contained within a 'nomad' tray filled by the pharmacist.
They are not even allowed to hand medication to their clients .
So, in answer to your question, I would follow the guidelines for caring.
If you are employed privately, I would get some guidelines in place pronto.
If I were 'helping out' I would have nothing at all to do with any medication tha had not been properly prescribed.
Not sure who you intend to 'report' this to ?
Local authority carers where I live will not give medication at all unless the mes are contained within a 'nomad' tray filled by the pharmacist.
They are not even allowed to hand medication to their clients .
So, in answer to your question, I would follow the guidelines for caring.
If you are employed privately, I would get some guidelines in place pronto.
If I were 'helping out' I would have nothing at all to do with any medication tha had not been properly prescribed.
Not sure who you intend to 'report' this to ?
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