JUSTICE 4 PAT MUM DIED HELP Change NHS RULE One dose fits all Levofloxacin has no antidote

The Issue

My mother went to hospital on 6th August 2017 for a urine infection she is dead!

 

The hospital did not feed her for 18 days, dehydrated her for 71 hrs, gave her maximum dose of levofloxacin this is a urine infection drug. 

 

It clearly states on medication administration to reduce dosage anyone over 65 to take into account fraylity fragility and weight of person. 

The NHS derriford hospital are giving 500g rule one dose for all rule to all the elderly as main urine infection drug. 

IF You Have  An Allergic Reaction you could die as  there is  No Antidote. 

The Dr called me on Wednesday 9th August 2017 and said "we've administered a medication to your mum it has caused two seizures to the brain within 30 mins of each other.  Has she ever had a seizure?"  I replied "never in her life"    he replied "we've took her off the medication now we are doing everything we can"  it was then said to me by Tuesday 15th August 2017 by Dr Hall "just accept she's dying she's had a good life" to which I replied "I want a second opinion"  the Dr then said "her Central nervous system.  Peripheral nervous system has broke down" to which I replied "what you give my mum?"  they would not tell me.  Another Dr then said "let her die we will do the investigation after she dies". 

 

They took my mum of sodium chloride and water on friday 18th August 2017.  I asked a female Dr why they administered the medication maximum dose and the fact my mum diabetic type 2 and on medication metformin glicazide paracetamol whether they took that medication into account before administering maximum dose of levofloxacin to my mum.  Did they take my mums weidht and fragility into account? To which she would not discuss.  I then asked why they did not feed her for 11 days when could of via canular or via stomach via peg feed to no avail. 

On the Sunday 19th August 2017  I was told we are not giving your mum water ans sodium chloride as it will prolong her death and save her life?? 

 

The senior consultant came back on Monday 20th August 2017 from holiday disgusted.  He said to me "I heard you have been living in the hospital by your mother's side since Wednesday 15th August 2017.  He then apologised on behalf of NHS and  then advised in all the years of doctoring the fact that he had never seen anyone have such a bad allegic reaction to this drug LEVOFLOXACIN.

Dr Hancock advised the NHS are giving this drug to all the elderly One dose for all at standard maximum dose 500mg when I asked why the weight and size of person is not being taken into account and following pharmaceutical guidelines?  I was advised that is the rule NHS has been advised to follow and TNERE is no Antidote to reverse any allergic reaction.  I then asked "So if any elderly get an allergic reaction or anyone and it triggers of massive side effects people die as nothing can reverse it.  To which he said" well quite possibly as no antidote, the NHS. Measure how many lives it helps save or assist against isolated incidents". To which I replied "you know my mum has been given 3 doses at maximum dose and her weight size was not taken into account and consequences she's now a cabbage and dying isn't she". To which he replied in front of my husband "unfortunately yes".  He then advised he did feel the medication has attributed to my mother's health deterioration and then said "on a humane level he would do everything in his power to save my mums life if he was able.

 

He immediately agreed in putting my mum back on drip for water and sodium chloride as soon as this done her fever and swelling of limbs went down.

 

He advised my husband and self that if he saw lmprovement over 4 consecutive days he would get food into my mum via canular via nutrients.  On day one Monday 20th August 2017  he put improvement. Day 2 Tuesday 21st August 2017 l asked my mother to fight to live and open her eyes and move them left to right.  She did then  the Dr asked her questions and she responded he called it a miracle.  Day three Wednesday 22nd August 2017 midazolam administered increased we saw improvement but Dr put no change as he needed to see improvement.  Day 4 Thursday 23rd August 2017 no improvement Day 5 Friday 24th August 2017 midazolam increased we saw improvement ie less sisures.  Day 6 Saturday 25th Auguist 2017 hardly any seizures Midazolam.

 

Sunday 27th August 2017 my mother died in my arms. 

The senior consultant Dr Hancock is and was a true gentleman as all the nurses and Carers.  And Dr Sibley.   Someone made decision to administer this drug at maximum dose.   Triggering massive side effects.  And now our mum is dead.  Death Comes to us all but not following pharmaceutical guidelines, and administering a drug knowing no antidote to reverse it surely as a family and daughter we deserve justice.  Not financial gain but for this drug to be stopped until antidote found to reverse any allergic reaction and tackle any side effects ie. 

 

Find Antidote and follow pharmaceutical guidelines. 

 

 

 

This petition had 138 supporters

The Issue

My mother went to hospital on 6th August 2017 for a urine infection she is dead!

 

The hospital did not feed her for 18 days, dehydrated her for 71 hrs, gave her maximum dose of levofloxacin this is a urine infection drug. 

 

It clearly states on medication administration to reduce dosage anyone over 65 to take into account fraylity fragility and weight of person. 

The NHS derriford hospital are giving 500g rule one dose for all rule to all the elderly as main urine infection drug. 

IF You Have  An Allergic Reaction you could die as  there is  No Antidote. 

The Dr called me on Wednesday 9th August 2017 and said "we've administered a medication to your mum it has caused two seizures to the brain within 30 mins of each other.  Has she ever had a seizure?"  I replied "never in her life"    he replied "we've took her off the medication now we are doing everything we can"  it was then said to me by Tuesday 15th August 2017 by Dr Hall "just accept she's dying she's had a good life" to which I replied "I want a second opinion"  the Dr then said "her Central nervous system.  Peripheral nervous system has broke down" to which I replied "what you give my mum?"  they would not tell me.  Another Dr then said "let her die we will do the investigation after she dies". 

 

They took my mum of sodium chloride and water on friday 18th August 2017.  I asked a female Dr why they administered the medication maximum dose and the fact my mum diabetic type 2 and on medication metformin glicazide paracetamol whether they took that medication into account before administering maximum dose of levofloxacin to my mum.  Did they take my mums weidht and fragility into account? To which she would not discuss.  I then asked why they did not feed her for 11 days when could of via canular or via stomach via peg feed to no avail. 

On the Sunday 19th August 2017  I was told we are not giving your mum water ans sodium chloride as it will prolong her death and save her life?? 

 

The senior consultant came back on Monday 20th August 2017 from holiday disgusted.  He said to me "I heard you have been living in the hospital by your mother's side since Wednesday 15th August 2017.  He then apologised on behalf of NHS and  then advised in all the years of doctoring the fact that he had never seen anyone have such a bad allegic reaction to this drug LEVOFLOXACIN.

Dr Hancock advised the NHS are giving this drug to all the elderly One dose for all at standard maximum dose 500mg when I asked why the weight and size of person is not being taken into account and following pharmaceutical guidelines?  I was advised that is the rule NHS has been advised to follow and TNERE is no Antidote to reverse any allergic reaction.  I then asked "So if any elderly get an allergic reaction or anyone and it triggers of massive side effects people die as nothing can reverse it.  To which he said" well quite possibly as no antidote, the NHS. Measure how many lives it helps save or assist against isolated incidents". To which I replied "you know my mum has been given 3 doses at maximum dose and her weight size was not taken into account and consequences she's now a cabbage and dying isn't she". To which he replied in front of my husband "unfortunately yes".  He then advised he did feel the medication has attributed to my mother's health deterioration and then said "on a humane level he would do everything in his power to save my mums life if he was able.

 

He immediately agreed in putting my mum back on drip for water and sodium chloride as soon as this done her fever and swelling of limbs went down.

 

He advised my husband and self that if he saw lmprovement over 4 consecutive days he would get food into my mum via canular via nutrients.  On day one Monday 20th August 2017  he put improvement. Day 2 Tuesday 21st August 2017 l asked my mother to fight to live and open her eyes and move them left to right.  She did then  the Dr asked her questions and she responded he called it a miracle.  Day three Wednesday 22nd August 2017 midazolam administered increased we saw improvement but Dr put no change as he needed to see improvement.  Day 4 Thursday 23rd August 2017 no improvement Day 5 Friday 24th August 2017 midazolam increased we saw improvement ie less sisures.  Day 6 Saturday 25th Auguist 2017 hardly any seizures Midazolam.

 

Sunday 27th August 2017 my mother died in my arms. 

The senior consultant Dr Hancock is and was a true gentleman as all the nurses and Carers.  And Dr Sibley.   Someone made decision to administer this drug at maximum dose.   Triggering massive side effects.  And now our mum is dead.  Death Comes to us all but not following pharmaceutical guidelines, and administering a drug knowing no antidote to reverse it surely as a family and daughter we deserve justice.  Not financial gain but for this drug to be stopped until antidote found to reverse any allergic reaction and tackle any side effects ie. 

 

Find Antidote and follow pharmaceutical guidelines. 

 

 

 

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The Decision Makers

Boris Johnson
Prime Minister
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Petition created on 31 May 2019