eHealthMe - Personalized health information & community eHealthMe - Personalized health information & community

Personalized health information & community

  Tools   Community
All drugs: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
All conditions: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Check symptoms       Compare drugs       Ask question       Write review       Answered/ Unanswered       Reviews

Review: could Furosemide cause Headache - migraine with aura (Migraine with aura)?

Summary: Headache - migraine with aura is reported only by a few people who take Furosemide.

We study 80,003 people who have side effects while taking Furosemide from FDA and social media. Among them, 2 have Headache - migraine with aura. Find out below who they are, when they have Headache - migraine with aura and more.

You are not alone: join a mobile support group for people who take Furosemide and have Headache - migraine with aura >>>

 

 

 

 

Furosemide

Furosemide has active ingredients of furosemide. It is often used in fluid retention. (latest outcomes from 80,851 Furosemide users)

Headache - migraine with aura

Headache - migraine with aura (silent migraine) has been reported by people with high blood pressure, birth control, depression, osteoporosis, migraine. (latest reports from 2,190 Headache - migraine with aura patients)

On Jan, 30, 2015: 80,003 people reported to have side effects when taking Furosemide. Among them, 2 people (0.00%) have Headache - Migraine With Aura.

Trend of Headache - migraine with aura in Furosemide reports

Time on Furosemide when people have Headache - migraine with aura * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Headache - migraine with aura0.00%0.00%0.00%0.00%0.00%0.00%100.00%

Gender of people who have Headache - migraine with aura when taking Furosemide * :

FemaleMale
Headache - migraine with aura50.00%50.00%

Age of people who have Headache - migraine with aura when taking Furosemide * :

0-12-910-1920-2930-3940-4950-5960+
Headache - migraine with aura0.00%0.00%0.00%0.00%0.00%0.00%0.00%100.00%

Severity of Headache - migraine with aura when taking Furosemide ** :

leastmoderateseveremost severe
Headache - migraine with aura0.00%100.00%0.00%0.00%

How people recovered from Headache - migraine with aura ** :

while on the drugafter off the drugnot yet
Headache - migraine with aura0.00%0.00%100.00%

Top conditions involved for these people * :

  1. Adhd (1 people, 50.00%)
  2. Migraine (1 people, 50.00%)
  3. Chronic myeloid leukaemia (1 people, 50.00%)
  4. Edema - peripheral, peripheral edema (1 people, 50.00%)
  5. Allergic rhinitis (1 people, 50.00%)

Top co-used drugs for these people * :

  1. Coumadin (2 people, 100.00%)
  2. Gleevec (1 people, 50.00%)
  3. Sumatriptan succinate (1 people, 50.00%)
  4. Lanoxin (1 people, 50.00%)
  5. Timoptic (1 people, 50.00%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Do you have Headache - Migraine With Aura while taking Furosemide?

You are not alone! Join a mobile support group:
- support group for people who take Furosemide and have Headache - Migraine With Aura
- support group for people who take Furosemide
- support group for people who have Headache - Migraine With Aura

Drugs in real world that are associated with:

Could your condition cause:

Can you answer these questions (Ask a question):

More questions for: Furosemide, Headache - migraine with aura

You may be interested at these reviews (Write a review):

  • Had nms in 2005, will trileptal increase chance of recurrence?
    In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
  • Cfs/fibro, migraine
    A strange thing happened when I started taking the Chantix for my smoking cessation...
    MY MIGRAINES AND TENSION HEADACHES WENT AWAY!!!
    As horrible as they were, and as bad as I have prayed for them to go away, I did not even notice that I didn't have the excruciating headaches anymore!!
    I stopped taking the chantix and the headaches gradually came back but it took me awhile to make this correlation. Once I did, I started taking the chantix again. it started working immediately... taking the migraines and neck pain away again! Now, I can take 1/2 of a pill every other day and that seems to keep the migraines away! There are side effects and I don't know if it would work for everyone but it sure worked for me!
  • Methadone maintenance and lichen planus
    Have been on methadone maint. since 1973 (with two brief periods of non use).

    Have suffered from Lichen Planus for the last 5 years with slow but steady progression of symptoms. Do not know when exposed to Hep C (IV drug use since 1968)and have been exposed to biohazardous materials from my career (lab director, Senior Microbiologist) since 1975.
  • Fibromyalgia & related health issues (3 responses)
    Fibromyalgia dx after pregnancy of only child at 42/other dx followed and seem to be in conjunction. heart issues did not appear until after the use of fibro meds- cymbalta, lyrica, neurontin, and more. had 1 seizure believed to be related to seretonin syndrome/years and years of mistreatment by doctors. unable to recall how many docs and meds through the years. one other very significant issue- after tooth extraction had puncture to left maxillary sinus-after YEARS of neglect by docs, found max. & ethmoid sinus completely opaque on CAT scan. Had surgery. Now, years later, have mucous plug that sporadically comes out upon sneezing. Fairly recent CAT scan shows sinuses again completely opaque. Certain needs further attention, but basically afraid to go through surgery again. Also- may have had heart attack. ER visit said no, but shortly after, had abnormal ekg. Again, neglect from docs. Am now active advocate for fm/chronic pain patients. Disgusted by the whole lack of interest of medical community. Looking for answers through my own research to try to find a way to improve quality of life...
  • Treating copd and kidney disease (1 response)
    My biggest problem is trying to keep my blood pressure at 110 to 140 diastolic and controlling constipation.

More reviews for: Furosemide, Headache - migraine with aura

Comments from related studies:

  • From this study (4 months ago):

  • I have been in pain and have suffered for over 7 years with muscle pain with cramping, aching, burning, stinging, pins/needles, weakness, numbness and paralysis, etc. I live with fatigue and utter exhaustion everyday and hate having to take medicine period, but have no choice in the matter. I know that this is something serious..I can feel it. I just have to get the Doctors, to find it...and fix whatever it is that is wrong.
    I am trying to find what is the root cause of it all, then I might be able to find some relief.."Lord Willing". I have always been a driven individual and love life. I am a fighter and a survivor, so I will continue forward..until I find a way to the answer.
    The pain level stays around 5 or 6 everyday and can be overwhelming at times, but I pray and I find relief for a moment..from The Lord. Grateful to be alive. Just want life to be normal again and to be able, to spend my time with my family that I have missed so much of.

    Reply

    Grace on Oct, 18, 2014:

    Sounds like Lyme disease to me. It's in all 50 States.

    Reply

NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

   

About - Terms of service - Privacy policy - Press - Testimonials - Contact us

 
© 2015 eHealthMe.com. All rights reserved. Use of this site constitutes acceptance of eHealthMe.com's terms of service and privacy policy.