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Review: could Albuterol cause Migraines (Migraine)?





Summary: Migraines is found among people who take Albuterol, especially for people who are female, 50-59 old, have been taking the drug for 2 - 5 years, also take medication Singulair, and have Asthma.

We study 54,111 people who have side effects while taking Albuterol from FDA and social media. Among them, 433 have Migraines. Find out below who they are, when they have Migraines and more.

You are not alone: join a mobile support group for people who take Albuterol and have Migraines >>>

Albuterol

Albuterol has active ingredients of albuterol. It is often used in asthma. (view latest outcomes from 54,799 users)

Migraines

Migraines (headache) has been reported by people with multiple sclerosis, birth control, depression, osteoporosis, pain.(latest reports from Migraines 47,043 patients)

On Nov, 29, 2014: 54,105 people reported to have side effects when taking Albuterol. Among them, 433 people (0.80%) have Migraines.

Trend of Migraines in Albuterol reports

Time on Albuterol when people have Migraines * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Migraines0.00%25.00%0.00%0.00%37.50%12.50%25.00%

Gender of people who have Migraines when taking Albuterol * :

FemaleMale
Migraines87.82%12.18%

Age of people who have Migraines when taking Albuterol * :

0-12-910-1920-2930-3940-4950-5960+
Migraines0.00%1.72%5.42%10.84%18.23%20.69%25.12%17.98%

Severity of Migraines when taking Albuterol ** :

leastmoderateseveremost severe
Migraines0.00%66.67%33.33%0.00%

How people recovered from Migraines ** :

while on the drugafter off the drugnot yet
Migraines0.00%50.00%50.00%

Top conditions involved for these people * :

  1. Asthma (100 people, 23.09%)
  2. Pain (75 people, 17.32%)
  3. Depression (44 people, 10.16%)
  4. Contraception (41 people, 9.47%)
  5. Gastrooesophageal reflux disease (37 people, 8.55%)

Top co-used drugs for these people * :

  1. Singulair (83 people, 19.17%)
  2. Nexium (80 people, 18.48%)
  3. Vicodin (73 people, 16.86%)
  4. Ativan (70 people, 16.17%)
  5. Valium (69 people, 15.94%)

* 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 Migraines while taking Albuterol?

You are not alone! Join a mobile support group:
- support group for people who take Albuterol and have Migraines
- support group for people who take Albuterol

Drugs in real world that are associated with:

Could your condition cause:

Can you answer these questions (Ask a question):

  • Why when i have a migraine i feel the need to eat more and more?
    Can someone please help me why when I get a migraine I have the need for excessive eating? I get the feeling that if I eat more I will feel better. I am now 43 years old woman and my migraines the last three years get worse and worse. Both more intense and more often ( like twice or even three times a week). I am on Effexor that is treating depression 75mg per day. Can someone advise me what can I do? I feel so much helpless and frustrated as my quality of life has deterioted so much.
    Reply
  • Is it ok to take fioricet and albuterol together?
    I have been having bad headaches the pain is behind my eyes front for head and temples (I have also had a warming sensation in the back of head and thought body here and there that no one can explain to me ) but I have been subscribed fioricet but I'm a chronic asthmatic so I take albuterol inhaler and some times solution for my neb I read that these 2 can have interation and I been feeling shortness of breath which I know can be a side effect from fioricet but I do take my inhaler daily and I want to check if anyone has been in same situation and if there were any interactions
    Reply
  • Is it my thyroid or am i mentally ill? diagnosed w/ hashimoto's thyroiditis but untreated - chronic pain unmanaged also (2 answers)
    I moved to OR from HI and brought all my records, signed releases, and had many diagnoses, all but the thyroid, was being treated and long-term. I also took Oxycontin & Oxycodone for severe chronic pain from bilateral SI joint fusion (right screw protrudes & leg also becomes numb and weak with activity) & lumbar and cervical degeneration & facet arthropathy. I had volunteered reducing dosage as I'm always trying to reduce Rx intake to alleviate side effects (I am tiny, even for a youth & adult dosages seem to drug me). Next month, it was known that I could not function well because pain was not managed, but needed to resolve it in OR, as moving. OR Drs. refused to return me to higher dosage (taking minimalist Oxycontin 10 mg CR & Oxycodone/Acet 5mg). After being unable to get up to go to bathroom, walk, contacted adult services to see about in home services & possible foster care placement for young son since I was losing independence & failing in general health & cognitive functioning. I was forced to take bottles of OTC Tylenol to function, with Dr's knowledge, & knowing I had past lesions on liver to follow. Several months later had follow up liver ultrasound, & new small lesions found on liver. After emailing dr about from DHS questioning failure to manage my pain vs. conditions that were disabiling, 6 months later, dr told me I was experiencing withdrawals every morning & finally agreed to increase Oxycontin to 15 mg, which has enabled me to tolerate the pain & function. I have been treated as a drug-seeking patient since attempting to transfer my care.
    I have multiple autoimmune conditions, most of which I no longer treat with Rx as I have been overmedicated & side effects are too numerous. So I actually am opposite in many ways. I stopped Lyrica, Silenor (sleep), Elmiron, Bentyl, Dexilant. Stress affects me seriously since I had a TBI and experience anxiety stress disorder, which seems to contribute to auto immune responses. But still knew triggers & familiar with self - this thyroid diagnosis & symptoms experienced new & too destabilizing to live.
    Diagnosed w/ Hashimoto's thyroiditis after 1/2 thyroid removed Nov 2011; my antibodies are unbelievably high. I declined in thinking, memory, anxiety-unable to think/track, losing most,getting lost driving, sleep very dysfunctional, too emotional, crying easily & often (unusual for me). I feared losing ability to live independently. My maintenance Rx (Silenor, Lyrica) seemed to drug me. I tried to explain to drs. that I needed thyroid replacement hormones that I never had these problems before.
    They referred me to a psychiatrist for medicine management consultation, who gave me mental health diagnoses (histrionic personality disorder, somatoform (hypochondria) that discredited me & ruined my medical records for future validity. Is it thyroid symptoms? Was unmanaged pain contributing? Too much Tylenol? What does a dysfunctional thyroid do to a person? How do I get my medical record addressed to reflect accuracy?
    Reply
  • I've stopped using salbutamol after 15yrs i now have symptoms of ulnar palsy
    i've taken 4 puffs of ventalin for around 15 years along with clenil, at a recent asthma checkup i was told to stop using the ventalin... asthma is well under control, but i am now experiencing forearm/elbow pain especially in the morning my ring and little fingers feel numb and tingle for a while my wrists seem weak and i often get pain when gripping. I'm now taking 6 ibuprofen daily and the symptoms have reduced a little. Are the symptoms a possible result of stopping the use of the ventalin -salbutamol?
    Reply
  • My ige in november was 1712, i have been diagnosed with late onset asthma, i get breathless at the slightest exertion e.g. waking to bathroom and back into bed; my iron levels are low (1 answer)
    I have late onset asthma, told two weeks ago that my iron levels are low, IgE of 1712 (Nov 2013), get breathless with little exertion (e.g. going to toilet and back into bed), I lose concentration easily. In August 2013 I lost my sense of smell, but I have been checked by ENT - no blockages. So what is the problem with me
    Reply

More questions for: Albuterol, Migraines

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    I have taken both Imitrex and Butalb/acet/caffeine and I have to say that Imitrex works far better than the other one! The substitute I was given for Imitrex doesn't even touch my migraine pain.
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  • Bad side effect of melatonin/imitrex use together
    I have taken melatonin for insomnia I've been experiencing recently (not a chronic condition). I haven't had any problems or interactions with my other regular medications while using the melatonin, other than drowsiness in the morning. Last night I had a migraine at bedtime, so took 50 mg. of imitrex, my usual dose for one. Since I haven't had one during the period I've been taking the melatonin I feel fairly confident in assuming that my symptoms were a result of the combination.



    I was awoken--thank god!--by choking on my own saliva and almost vomiting. I was able to go back to sleep--lying on my side to avoid aspirating anything--and was awoken again several hours later while I was wetting the bed!!! Incontinence has never been an issue for me (well, not since I was 3, I imagine) and I was really shocked. Although I immediately got up to clean the bed, I was so sleepy that I got back in (on the dry side :) and slept for another 4 hours.



    Although, as I mentioned, I think it's likely that the problem was the result of an interaction with the Imitrex, which has a soporific effect, I'll stop using the melatonin to be safe!
    Reply
  • My reaction to talking sumatriptan for the first time.
    after 10 minutes of taking the sumatriptan tablet i got all of the symptoms i stated and from those i developed a rare movement disorder called 'Dystonia' that has affected my right foot making me unable to walk and my right hand making me unable to write.
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More reviews for: Albuterol, Migraines

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