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Lyme Disease ForumsGeneral & SupportDont know what to do
05/25/2012 04:25 PM
Bettyg
 
Posts: 26579
VIP Member
I'm an Advocate

vick, where did you get info, specific link please, about pepto bismal can cause BLINDNESS?|

i checked NIH'S MEDICAL LIBRARY finding this; NOTHING is mentioned about this as being severe side effect???

http://www.nlm.nih.gov/medlineplus/druginfo/meds/ a607040.html

bettyg, iowa activist

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
Reply

05/25/2012 06:09 PM  Top
RavenLunatic
RavenLunatic
 
Posts: 2597
Group Leader

Betty - Here's a link to Pepto Bismal causing possible blindness.

Drugs.com states that long-term use of Pepto Bismol might cause encephalopathy, which according to the National Institutes of Neurological Disorders is a condition characterized by altered brain function and structure. Signs and symptoms of encephalopathy include confusion, hallucinations, seizures, dulling of senses, coma and, on occasion, blindness. Encephalopathy can cause permanent brain damage.

Read more: http://www.livestrong.com/article/241982-side-effects-of- pepto-bismal-chewable-tablets/#ixzz1vvwTVeV0

Post edited by: RavenLunatic, at: 05/25/2012 06:09 PM

Post edited by: RavenLunatic, at: 05/25/2012 06:10 PM

"My Disabling, Chronic Illness Is More Real Than Your Imaginary, Medical Expertise!!!"

05/26/2012 12:37 AM  Top
Bettyg
 
Posts: 26579
VIP Member
I'm an Advocate

vick and RAVEN, thanks so much D for finding that link and posting it.

NEVER HEARD THAT; i was shocked to see that there!

think i'll add this thread to my meds/treatment index so other might be able to find it if need be!

bettyg, iowa activist

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
Reply

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