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User Voices for Fosamprenavir Calcium

The following are comments from users that experienced side effects while taking Fosamprenavir Calcium

Irritability

It seamed to make me grouchy so I stopped using it


Source: Wellbutrin

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Fatigue

Have been on for a couple of years and it helped me get over the depression/ zero energy hump. I hope Vyvanse will get me over the ADD hump


Source: Wellbutrin

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Paranoia

very paranoid on this


Source: Wellbutrin

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Sleep Disorder

Sleep problems and stance dreams


Source: Wellbutrin

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Drug Ineffective

not worked


Source: Wellbutrin

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Disturbance In Attention

I'm taking this med, but I wish I could get on something better for ADHD because I really have bad concentration .


Source: Wellbutrin

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Hallucination, Auditory

working this has worked great for me except too much of it causes me to hear voices so when I am getting down I need an extra antidepression.


Source: Wellbutrin

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Depression

take in concert with other anti depressants and mood stabilizers


Source: Wellbutrin

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Drug Tolerance Increased

Worked for awhile in addition to paxil. Stopped working and changed medication.


Source: Wellbutrin

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Drug Tolerance Increased

stopped working


Source: Wellbutrin

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Depression

Helps with the depression but has made my essential tremor and Tourette's worse. Had to drop it due to healthcare issues.


Source: Wellbutrin

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Did the author experience depression while taking fosamprenavir calcium?

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Essential Tremor

Helps with the depression but has made my essential tremor and Tourette's worse. Had to drop it due to healthcare issues.


Source: Wellbutrin

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* 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.