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Atripla Related Hypersensitivity

Official Government Database Reports24
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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.


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Druginformer Identified Side Effects: Flatulence, Photophobia, Malaise, Hypersensitivity, Abnormal behaviour, Tinnitus, Thought withdrawal, Confusional state, Depersonalisation, Disturbance in attention, Somnolence, Weight increased, Adverse drug reaction, Negative thoughts, Appetite disorder, Flatulence, Photophobia, Malaise, Hypersensitivity, Abnormal behaviour, Nightmare, Tinnitus, Adverse event, Thought withdrawal, Confusional state, Depersonalisation, Disturbance in attention, Somnolence, Adverse drug reaction, Negative thoughts, Appetite disorder

Posted By Anonymous in askapatient.com on March 17, 2011 @ 12:00 am

... meaninglessness leading almost to a sense of but not a full fruition of depersonalization; malaise; fuzziness/tinnitus associated with eating high fat meals; increased flatulence; decreased ability to...

Druginformer Identified Side Effects: Flatulence, Photophobia, Malaise, Hypersensitivity, Abnormal behaviour, Tinnitus, Thought withdrawal, Confusional state, Depersonalisation, Disturbance in attention, Somnolence, Weight increased, Adverse drug reaction, Negative thoughts, Appetite disorder, Flatulence, Photophobia, Malaise, Hypersensitivity, Abnormal behaviour, Nightmare, Tinnitus, Adverse event, Thought withdrawal, Confusional state, Depersonalisation, Disturbance in attention, Somnolence, Adverse drug reaction, Negative thoughts, Appetite disorder

Posted By Anonymous in askapatient.com on March 17, 2011 @ 12:00 am

... meaninglessness leading almost to a sense of but not a full fruition of depersonalization; malaise; fuzziness/tinnitus associated with eating high fat meals; increased flatulence; decreased ability to...

Druginformer Identified Side Effects: Hypersensitivity

Posted By SeanCA in fdb.rxlist.com on June 17, 2010 @ 12:00 am

The once-a-day regime was a big selling point, unfortunatley I was allergic to the sustiva and had to discontinue use after only two days.

Druginformer Identified Side Effects: Hypersensitivity, Hypersensitivity

Posted By lorij3 in www.dailystrength.org

I had a severe allergic reaction and had to stop taking i

Druginformer Identified Side Effects: Nausea, Hypersensitivity, Nightmare, Urticaria, Somnolence, Nausea, Hypersensitivity, Nightmare, Urticaria, Somnolence

Posted By wolfette in www.dailystrength.org

I was allergic to Atripla. I had the nightmares, nausea, and tiredness. But the side effect that we stopped it for was Severe Hives. We tried Benadryl with it but then I actually nodded off four ti...

Druginformer Identified Side Effects: Hypersensitivity, Hypersensitivity

Posted By cahirtodat89 in www.dailystrength.org

I had an allergic reaction, but at this moment my doc has me off meds since my numbers are good

Druginformer Identified Side Effects: Nausea, Hypersensitivity, Nightmare, Urticaria, Somnolence, Nausea, Hypersensitivity, Nightmare, Urticaria, Somnolence

Posted By wolfette in www.dailystrength.org

I was allergic to Atripla. I had the nightmares, nausea, and tiredness. But the side effect that we stopped it for was Severe Hives. We tried Benadryl with it but then I actually nodded off four ti...

Druginformer Identified Side Effects: Hypersensitivity, Hypersensitivity

Posted By cahirtodat89 in www.dailystrength.org

I had an allergic reaction, but at this moment my doc has me off meds since my numbers are good

Druginformer Identified Side Effects: Hypersensitivity, Hypersensitivity

Posted By lorij3 in www.dailystrength.org

I had a severe allergic reaction and had to stop taking i


* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.