Review: could Lariam cause Cfs?
We study 2,900 people who have side effects while taking Lariam from FDA and social media. Among them, 9 have Cfs. Find out below who they are, when they have Cfs and more.
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Lariam (latest outcomes from 2,933 users) has active ingredients of mefloquine hydrochloride. It is often used in malaria.
Cfs (chronic fatigue syndrome) (latest reports from 12,956 patients) has been reported by people with acne, depression, high blood pressure, high blood cholesterol, pain.
On Jul, 8, 2014: 2,900 people reported to have side effects when taking Lariam. Among them, 9 people (0.31%) have Cfs. They amount to 0.07% of all the 12,843 people who have Cfs on eHealthMe.
Time on Lariam when people have Cfs * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Cfs when taking Lariam * :
Age of people who have Cfs when taking Lariam * :
Severity of Cfs when taking Lariam ** :
How people recovered from Cfs ** :
Top conditions involved for these people * :
- Malaria prophylaxis (3 people, 33.33%)
- Depression (1 people, 11.11%)
Top co-used drugs for these people * :
- Zoloft (2 people, 22.22%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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From this study (10 hours ago):
I have so many side effects that chronic fatigue seems simplistic. Almost every cell in my body has been damaged. I have seen over 20 doctors since my cascade of symptoms started (13years ago). They all play dumb, tell me my problem is not in their specialty, or offer me antidepressants. Yet when I look up actual research, I see that most of the pieces of the physiology of my syndrome have been known for years (some for decades).
I also note that on this web site, there is no way to report a high number of side effects or simplify them as mitochondrial damage.
I believe it is the intent of this web site, the AMA, drug companies, and most doctors to deliberately avoid "knowing" about the holocaust of poisoning that is occurring in the name of heath care.
The logarithmical explosion of cancer, obesity, depression, allergies, auto-immune diseases, "rare genetic diseases," and diabetes (to name just a few) matches exactly the explosion of pharmaceutical consumption.
It would be appropriate to apply the scientific method instead of the profit motive to further human health.
kilo on rappahannock on Jul, 7, 2014:
Doxy and azithromycin both can cause mitochondrial damage. Both were prescribed, taken, and began my problems before I got Lyme and was treated with yet more doxy, which caused even more serious mitochondrial damage. Large doses of ubiquinol allow my to function at a passible level.
Any and all antibiotics damage your immune system and can allow further infections. Some cause mitochondrial damage. Many other drugs can also cause mitochondrial damage. A huge number of drugs have been recently given black box warnings for anyone with mitochondrial disease. It is also true (though not yet admitted by the FDA) that many of those drugs can cause the mitochondrial damage in the first place.
noscreenname on Jul, 6, 2014:
you know, negative test does not EVER mean no lyme. This is how it works: most tests look for the actual bug; not the lyme test. Lyme test looks for your antibodies to lyme. In raging lyme, bacteria far outnumber the antibodies you can make to fight it. Think of each antibody, as a key that fits in a germ's lock. Once met, the two die together - the antibody can no longer 'react' on the test. test uses dead lyme bacteria, and waits for antibodies to latch on, = positive. Raging infection = millions of busy antibodies, cant register this test. ONLY recovering lymies usually see the positive tests, because antibiotics have now put a dent in the bacterial population.
NEVER ever rely on a negative lyme test. All docs ought to know this. The lab report directs them with these words, as well. Symptoms = #1 diagnosis for lyme. and for you and anyone else reading: ELISA test, is for rash stage. BLOT, is for anything after the first month. My son, got a lyme rash from mosquito bites midwest - he was treated on the spot, with lyme abx -- guess what? 20 days later, broke out in bartonella stripes, looks like stretch marks - lyme brings with it other bacteria, 10 of them if you look it up, almost more often than the lyme bacteria itself = and none of them, respond to the lyme meds - they all need different meds. Hence, if you had the bullseye rash, were treated with doxy etc, you could have the other co infections that dont respond to doxy etc and need a specialist. Doxy shouldnt cause any damage like youre describing. If it made you feel ill, this is called a herxheimer reaction and indicates bacterial die off. (I could not stand doxy when first found with lyme advanced - made me 300% worse while on it, but its a good sign).
kilo on rappahannock on Jun, 27, 2014:
I did have lyme, but it was treated immediately at the appearance of the classic rash. I have been tested several times since - always negative. I looked up mycoplasma and serratia, as you suggested, but found almost none of the symptoms apply to my problems. Thank you for the information. I can now pass that info on to anyone with those sort of symptoms. My symptoms can all be explained by mitochondrial damage caused by doxycycline and azithromycin. Thanks again for your reply. We all need to teach each other as much as possible, as the doctors won't do it.
noscreenname on Jun, 23, 2014:
if you have lyme, youre 75% of 100 likely to have either mycoplasma, or serratia. these cause kidney stones, which in turn, cause damage or loss if not surgically removed (struvite type) AND the way the spirochete and other partner bacteria hide from the meds. The lyme docs have known this all along when they said, "it hides where meds cannot get to it". 75% of lymies having myco...= struvite stones that will keep ANY coinfections going on indefinitely via relapse. Its all about meal ticket patients here....sad.
From this study (6 days ago):
For the last 3 years in the spring, I have developed a severe cough and peripheral edema. I was hospitalized for this 2 years ago when the cough wouldn't resolve and the edema became cellulitis. Antibiotics help with the cough, but the edema persists. Never had this so late in the year, usually resolved by now.
aimhigh4once on Jul, 2, 2014:
I had been taking nasonex for about 16 months on and off when the insurance wouldn't approve it any longer....then I was able to get approval after 2 months of being off of it. (filled scrip in dec 2013) I used it everyday. I was not taking anything else except ibuprofen on and off when needed. I continued to get sicker. I had headaches, eye pain, ear pain, sore throats and a swishing sound like a heart beat. It went on to cause short term memory loss and confusion. I was diagnosed with Idiopathic Intracranial Hypertension with papilledema. I found 2 articles that talked about steroidal usage as a cause for IIH with paps. I looked up Nasonex and found it was a steroidal spray. I stopped taking it on June 19, 2014 and for the last 3 days I have had no double vision, and no swishing in my ears.....I am hoping the rest of the symptoms will subside with time. I strongly suggest anyone taking this medication to do so with the ut most caution.
From this study (1 week ago):
I have been diagnosed with Primary biliary cirrhosis..wondering if this drug aggrevated or caused it
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On eHealthMe, Lariam (mefloquine hydrochloride) is often used for malaria. Find out below the conditions Lariam is used for, how effective it is, and any alternative drugs that you can use to treat those same conditions.
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