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User Voices for Tadalafil

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

Visual Impairment

Side Effects: After 2 1/2 months of taking cialis , vision began blurring in left eye and began developing mild pain and stiffness in lower neck and upper back. About 10 days later I had a stroke like...


Source: CIALIS: Side effects, ratings, and pat...

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Visual Impairment

... and pain is no longer experienced.Only SEVERE eye condition remains.

Hoping your research department can give me significant answers to the problems with my eyes ..Please contact me at your Q...


Source: CIALIS: Side effects, ratings, and pat...

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Visual Impairment

Side Effects: Clogged feeling, very heady and some back pain occasionally. Vision a little blurred on occasions. 20mg is a disaster, but 10mg is good for a couple of days. 5mg the day after keeps th...


Source: CIALIS: Side effects, ratings, and pat...

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Visual Impairment

Side Effects: large volume of clear ejaculate, distance shooting, flushed, nasal congestion, visual disturbance (temporary)

has anyone else found Cialis (as opposed to Viagra which had no s...


Source: CIALIS: Side effects, ratings, and pat...

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Visual Impairment

... multiple times over 2 days on only 2 - 20mg pills. Better than Viagra and Levitra but won't take again due to the severe side effects that last forever. Had a couple of vision issues within an hour o...


Source: CIALIS: Side effects, ratings, and pat...

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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.