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User Voices for Ciprofloxacin

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

Dry Skin

makes my mouth very dry , tired all the time


Source: Cipro

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Somnolence

makes my mouth very dry , tired all the time


Source: Cipro

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Discomfort

very sick !


Source: Cipro

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Candidiasis

I had it in the hospital IV for 6 days and a week P.O. after that. It helped, but gave me thrush !


Source: Cipro

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Fatigue

I hated taking this med. It made me tired and nauseated. I was on it for 3 months.


Source: Cipro

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Nausea

I hated taking this med. It made me tired and nauseated . I was on it for 3 months.


Source: Cipro

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Diarrhoea

Fine...maybe diarrhea , hard to tell...


Source: Cipro

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Pain

Took Cipro and Flagyl and was very nauseous and had a constant upset tum but it cleared up the pain on the left side. Still can't eat anything without it going right through me.


Source: Cipro

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Nausea

Took Cipro and Flagyl and was very nauseous and had a constant upset tum but it cleared up the pain on the left side. Still can't eat anything without it going right through me.


Source: Cipro

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Appetite Disorder

Took Cipro and Flagyl and was very nauseous and had a constant upset tum but it cleared up the pain on the left side. Still can't eat anything without it going right through me.


Source: Cipro

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Abscess

First attack was hospitalized. I had abscessed so no food IV antibiotics. Everything worked but had another attack about 4 months later. Again no food and biotics everything worked.


Source: Cipro

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Dizziness

made me feel very dizzy , but it did work well


Source: Cipro

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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.