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Patient Leaflet Updated 04-Jan-2022 | Martindale Pharma, an Ethypharm Group Company
Morphine 10mg/5ml Oral Solution
PACKAGE LEAFLET: INFORMATION FOR THE USER
Morphine 10mg/5ml Oral Solution
Morphine Sulfate
This medicine contains morphine sulfate which is an opioid, which can cause addiction. You can get withdrawal symptoms if you stop taking it suddenly.
Read all of this leaflet carefully before you are given this medicine because it contains important information for you.
Keep this leaflet, you may need to read it again
If you have any further questions, please ask your doctor, pharmacist or nurse.
If you get any side effects, talk to your doctor, or pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.
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What is In this leaflet:
1. What Morphine Oral Solution is and what it is used for
2. What you need to know before you take Morphine Oral Solution
3. How to take Morphine Oral Solution
4. Possible side effects
5. How to store Morphine Oral Solution
6. Contents of the pack and other information
1. What Morphine Oral Solution is and what it is used for
This medicine has been prescribed for you for the relief of severe pain.
It contains Morphine Sulfate which belongs to a class of medicines called opioids, which are 'pain relievers'. This medicine has been prescribed to you and should not be given to anyone else.
Opioids can cause addiction and you may get withdrawal symptoms if you stop taking it suddenly. Your prescriber should have explained how long you will be taking it for and when it is appropriate to stop, how to do this safely. Buy Morphine 10mg/5ml Oral Solution UK
2. What you need to know before you are given Morphine Oral Solution
Do not take Morphin
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The present study evaluated, using a well-controlled dehydration protocol, the effects of 24 h fluid deprivation (FD) on selected mood and
physiological parameters. In the present cross-over study, twenty healthy women (age 25 (SE 0·78) years) participated in two randomised
sessions: FD-induced dehydration v. a fully hydrated control condition. In the FD period, the last water intake was between 18.00 and 19.00
hours and no beverages were allowed until 18.00 hours on the next day (23-24 h). Water intake was only permitted at fixed periods during
the control condition. Physiological parameters in the urine, blood and saliva (osmolality) as well as mood and sensations (headache and
thirst) were compared across the experimental conditions. Safety was monitored throughout the study. The FD protocol was effective as
indicated by a significant reduction in urine output. No clinical abnormalities of biological parameters or vital signs were observed,
although heart rate was increased by FD. Increased urine specific gravity, darker urine colour and increased thirst were early markers
of dehydration. Interestingly, dehydration also induced a significant increase in saliva osmolality at the end of the 24 h FD period but
plasma osmolality remained unchanged. The significant effects of FD on mood included decreased alertness and increased sleepiness, fatigue
and confusion. The most consistent effects of mild dehydration on mood are on sleep/wake parameters. Urine specific gravity appears to
be the best physiological measure of hydration status in subjects with a normal level of activity; saliva osmolality is another reliable and noninvasive
method for assessing hydration status.