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User Voices for Fosamprenavir Calcium

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

Memory Impairment

I love it...it helps a lot but it makes me feel forgetful .


Source: Wellbutrin

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Tremor

Wellbutrin-my hands were shaking ,,could not sleep. Did cut down the cigarettes while on it.


Source: Wellbutrin

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Sleep Disorder

Wellbutrin-my hands were shaking,, could not sleep . Did cut down the cigarettes while on it.


Source: Wellbutrin

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Dependence

Still using. Ony difference I've noticed is it makes me calmer. But the cravings for nicotine still come.


Source: Wellbutrin

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Tinnitus

... caused by Cymbalta (and Paxil, and Celexa when I trid those). Works well enough in that respect, but also gives an added lift which I appreciate. Unfortunately, set off Tinitus in one ear (althoug...


Source: Wellbutrin

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Weight Decreased

Made me a psychopath but I lost weight on it


Source: Wellbutrin

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Drug Ineffective

Didn't work .


Source: Wellbutrin

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Diarrhoea

had to stop taking it, it gave me terrible stomach pain. not like diarhea , just sharp pains!


Source: Wellbutrin

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Pain

had to stop taking it, it gave me terrible stomach pain . not like diarhea, just sharp pains !


Source: Wellbutrin

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Abdominal Discomfort

had to stop taking it, it gave me terrible stomach pain . not like diarhea, just sharp pains!


Source: Wellbutrin

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Drug Ineffective

didn't really work for me


Source: Wellbutrin

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Drug Ineffective

It helps most days but somedays no help at all


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.