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Review: could Magnesium sulfate cause Ringing in the ears (Tinnitus)?

Summary: Ringing in the ears is found among people who take Magnesium sulfate, especially for people who are female, 60+ old, have been taking the drug for 1 - 2 years, also take medication Prilosec, and have Localised osteoarthritis.

We study 7,059 people who have side effects while taking Magnesium sulfate from FDA and social media. Among them, 40 have Ringing in the ears. Find out below who they are, when they have Ringing in the ears and more.

You are not alone: join a mobile support group for people who take Magnesium sulfate and have Ringing in the ears >>>

 

 

 

 

Magnesium sulfate

Magnesium sulfate has active ingredients of magnesium sulfate. It is often used in constipation. (latest outcomes from 7,306 Magnesium sulfate users)

Ringing in the ears

Ringing in the ears (a ringing in the ears) has been reported by people with depression, high blood pressure, high blood cholesterol, osteoporosis, stress and anxiety. (latest reports from 19,987 Ringing in the ears patients)

On Jan, 29, 2015: 7,055 people reported to have side effects when taking Magnesium sulfate. Among them, 40 people (0.57%) have Ringing In The Ears.

Trend of Ringing in the ears in Magnesium sulfate reports

Time on Magnesium sulfate when people have Ringing in the ears * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Ringing in the ears0.00%33.33%0.00%33.33%33.33%0.00%0.00%

Gender of people who have Ringing in the ears when taking Magnesium sulfate * :

FemaleMale
Ringing in the ears69.23%30.77%

Age of people who have Ringing in the ears when taking Magnesium sulfate * :

0-12-910-1920-2930-3940-4950-5960+
Ringing in the ears0.00%0.00%0.00%0.00%3.33%3.33%33.33%60.00%

Severity of Ringing in the ears when taking Magnesium sulfate ** :

leastmoderateseveremost severe
Ringing in the ears0.00%100.00%0.00%0.00%

How people recovered from Ringing in the ears ** :

while on the drugafter off the drugnot yet
Ringing in the ears0.00%0.00%100.00%

Top conditions involved for these people * :

  1. Localised osteoarthritis (8 people, 20.00%)
  2. Neuralgia (4 people, 10.00%)
  3. Generalized anxiety disorder (4 people, 10.00%)
  4. Back pain (4 people, 10.00%)
  5. Type 2 diabetes mellitus (4 people, 10.00%)

Top co-used drugs for these people * :

  1. Prilosec (16 people, 40.00%)
  2. Synthroid (13 people, 32.50%)
  3. Reglan (13 people, 32.50%)
  4. Vioxx (12 people, 30.00%)
  5. Ambien (12 people, 30.00%)

* 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 Ringing In The Ears while taking Magnesium Sulfate?

You are not alone! Join a mobile support group:
- support group for people who take Magnesium sulfate and have Ringing In The Ears
- support group for people who take Magnesium sulfate
- support group for people who have Ringing In The Ears

Drugs in real world that are associated with:

Could your condition cause:

Can you answer these questions (Ask a question):

  • How long ringing in ear after stopping drugdiclofenac
    ringing in ears how long before it goes away after stopping drug,diclofenac
  • Does clonazapam cause tinnitus or ringing in the ears?
    Patient fell a year ago and injured her neck and broke a bone in her arm. Has had severe pain in her neck. Getting acupuncture frequently. Recently tried to change medication from Valium to Clonazepam, and developed severe tinnitus. She said she only missed two days of Valium. She also says she has skipped days without taking valium and never had a problem. She says Clonazepam caused the tinnitus. I can't find anything that states a side effect of clonazepam is tinnitus.
  • Can xeralto and an antihistimine cause dizziness, shortness of breath, tiredness, etc.
    I also take a blood thinner, xeralto, for a-fib. I have been using a mouthwash of an antihistimine antacid mix for a day and a half.
  • Would the tinnitus abate with if i discontinue methotrexate?
    I've just begun my 4th year of Methotrexate for Rheumatoid issue, but it also alleviated my psoriasis. I am hesitant to discontinue because the benefits are great. However, the tinnitus is becoming unbearable and almost maddening. I will more likely consider talking to my doctor about changing medications if 1. The tinnitus subsides with the discontinuance of Methotrexate and if 2. Other rheumatoid medication would not have the same issues with tinnitus. Just discovered the possible connection minutes ago and am eager and hopeful. Please help. Thank you. -Celeste
  • Does anyone have persistent, ringing tinnitus while taking this drug? (1 answer)
    I was prescribed Atenolol years ago for tachycardia. I took it for many years with little to no side effects, aside from tiredness. I began having PVCs and later was diagnosed with Type 2 Diabetes. My doctor put me on 5 mg. Bystolic and the tinnitus started. I took it about 1 year. My BP wasn't ideal, so he upped it to mg. and the ringing worsened. It's much louder. The report says this drug isn't ototoxic, but I never had tinnitus before taking it. Anyone else????

More questions for: Magnesium sulfate, Ringing in the ears

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

  • Ringing in the ears from linzess
    I started Linzess about a month ago, taking it about every three days. It was my miracle pill, until recently when I started having ringing in my ears. I am stopping the medication in hopes that the ringing will subside.
  • Side effects of using terazosin
    I have been on terazosin for 9 days. The ringing in my ears is unbearable, dizzy in the night if I wake up to use the bathroom, intermittent throbbing heartbeat. Also very significant is dramatic decrease in libido and difficulty achieving satisfaction. Dose started at 5 mg at night, reduced to 2 mg. at night after two days and ringing does not go away. I have permission from my doctor to discontinue use and replace with Lisinopril.
  • Still ill after several years (1 response)
    I became ill several years ago.
    It all started with a head cold that lasted a few months and left me with Tinnitus and chronic sinusitis.

    After a nose operation and many visits to the doc and hospital, I am no closer to felling better or being cured.
    My doc gave me Beconase Aq at first and this made me very unwell, causing me fatigue which would last for a few days. I'm still searching for help.
  • Ringing in ear after kenalog injection
    After receiving a Kenalog injection, my son's left ear started a low pitch ringing after three days from the injection. Also his lower lip has quivered several times as well. This condition has lasted for nine days and I am looking for other patients who have had a similar reaction from a Kenalog injection.
  • Rocephin and levaquin drug interactions (1 response)
    I went to ER of local hospital because I was feeling puny, low energy for a while. I was on no meds, physical active all my life, yoga practiser, no crippling. I am late deafened, can speak clearly. This is a true case of attempted murder. I refused to admit myself after waiting 8 hours - I was refused the ability to leave - I was not sick enough - they only suspected pneumonia. This is a rural local hospital who can't get enough patients. I requested a certain antibiotic if one was needed that I tolerate well. It was a terrifying experience because they ignored everything I requested - especially to leave. I experienced burning pain at IV site, hand became inflamed, lost use of my thumbs, then legs would not support me. Could not brush hair or teeth. No one answered my questions about this crippling - it was a nightmare. I lost 16 pounds, my muscles were hanging off my body. I was released after 7 days, totally crippled with no directive or any explanation for these sudden excruciating pains and crippling. They refused me my records for a long time. No new doctor would discuss these records once I got them - every organ in body was visited with electrical like jolts, pain that no pain killers were effective on. In those records I find I had CHF, respiratory failure after 4 days of treatment. I find that they gave me mega doses(500/600 mg) Prednisone - remember - I was on nothing prior. NSAID's were given - three different ones, over 4,000mg daily. I was also given an injection of Fentanyl - 100 times stronger than morphine AFTER I refused to admit myself. My pain level in admitting was rated mild. I started coding - which, beig HOH, I did not know and was not told - after four days treatment . They ignored my inflamed hand(IV port), my complaints of burning at site, then all over. I was never told what I was given. It was horrifying to experience the pains I did after release. I had all new RX's so I did not know I had been given Levaquin - but I did not know hat Levaquin was anyway. I have marked PTSD because over the period of a couple of years - I find all those physicians and specialist who were purporting to be 'clueless' as to what happened to me - why I was suddenly crippled - they were lying or totally incompetent. I was given many other drugs - sedatives - cancer drugs mostly. I was prescribed a Z-pac upon release - all these inhibit breathing - cause heart failure. These are known dangers - murder indeed. My life is altered to the point I am home bound and can't care for myself or my pets, yard, house, garden. Why is this allowed to happen? $$$/profits for medical care - no accountability. Prednisone at mega lethal doses?? No medical care giver has a problem with this?? Oh, QIO states Levaquin is not a black boxed drug nor would giving mega doses Pred and NSAID's cause any problem.....he either can't read or is a liar. He is paid with Federal funds - they don't even try to cover up - its systemic in medical care. And carried out by our government - to accountability whatsoever.

More reviews for: Magnesium sulfate, Ringing in the ears

Comments from related studies:

  • From this study (6 days ago):

  • no i am not genetically predisposed for these conditions and all blood tests done with embolism causes have come back negative. majority of effects began with taking Remeron and Prazosin combo. was not diagnosed at all for high blood pressure for Prazosin Rx, actually had normal bp. after getting off Prazosin because of complete disorientation and blackouts, continued on Remeron and continued to get worse and worse depression with thoughts escalating to suicide. doctors have been very difficult in regards to this matter because they have so many clients on this junk and they do not want to lose their kickbacks and holidays from the drug companies but all i hear at the hospitals from other patients is how shitty and how many physical health issues occur while on Remeron/mirtazapine. there needs to be more medical awareness in regards to these products and the research needs to go far beyond "newest is best" mentality. my life is ruined because the prescribing doctor did not even want to monitor as directed for over a year and a half and did not want to heed medically apparent warning signs because it is not spelled out clearly enough that they have to be responsible for their patients conditions. now i run into an issue where my work compensation claim is being denied in regards to the physical side effects despite the recent reports from eHealthMe and FDA because the insurance company claims that there is not enough evidence and no definitive direction from the drug companies. only positive, am now slowly begining to lose weight since extremely hard battle while on remeron/mitazapine including near starving self to stop gaining weight. does anyone have any idea as to how to deal with this with a shortened life span and lifetime Rx for warfarin now demanded on top of possible surgeries and multiple procedures? is there anymore reports or doctors that understand what is going on as i am recieving pressure to continue on again with more antidepresents? what are the official list of "blood dissorders" referred to in the data and medical references about remeron/mirtazapine? is sleep deprivation and nightmares even an authorized/indicated use for Prazosin and if not why are psychiatrists and docs really pushing it for such a use? i am upset but any help with info would be great as i need to know how to deal with my current conditions and i believe the only way to do that is to reach a complete understanding about what went on before i am talked into drugging up a again with medical staff that does not want to acknowledge or educate about side effects and greater potential harm?

    Reply

  • From this study (1 week ago):

  • Geltimans disease

    Reply

  • From this study (2 weeks ago):

  • ear ringing started suddenly, not gradually.

    Reply

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