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Ciprofloxacin Related Hyperacusis

Official FDA Reports57
Social Media Events4

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Ciprofloxacin.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

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

Cipro

Side Effects: permanent neuropathy in the nerves of my skin. Numbness, tingling, cold burning pain. Tinnitus and extreme sensitivity to sound (hyperacusis) . Completely messed up my life. i took t...


Source:" CIPRO: Side effects, ratings, and pati...

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Did the author experience hyperacusis while taking cipro?

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Cipro

Side Effects: Tinnitus(ear-ringing), Hyperacusis ,Insomnia,Tendon & muscle pain,feelings of death & doom,hallucinations,it goes on & on & on.....

Its been over 2 years since I took the evil p...


Source:" CIPRO: Side effects, ratings, and pati...

View full report on drug related hyperacusis

Did the author experience hyperacusis while taking cipro?

What is this?

Cipro

Side Effects: Insomnea,Headaches, tinnitus(ear-ring)hyperacusi(sound sensitivity)Torn rotator cuff(shoulder)Plantar Fascias(feet)eye issue,stomach issues....the list goes on & on with Cipro ....WAS A H...


Source:" CIPRO: Side effects, ratings, and pati...

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Tell us about your Experience with Ciprofloxacin Related Hyperacusis

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Druginformer Identified Side Effects: Feeling cold, Hyperacusis, Burning sensation, Hypoaesthesia, Hypersensitivity, Neuropathy peripheral, Tinnitus, Anxiety, Adverse event, Paraesthesia

Posted By Anonymous in askapatient.com on January 24, 2015 @ 12:00 am

Side Effects: permanent neuropathy in the nerves of my skin. Numbness, tingling, cold burning pain. Tinnitus and extreme sensitivity to sound (hyperacusis). Completely messed up my life. i took t...

Druginformer Identified Side Effects: Hyperacusis, Myalgia, Tinnitus, Accidental poisoning, Death, Hallucination, Insomnia

Posted By Anonymous in askapatient.com on November 9, 2009 @ 12:00 am

Side Effects: Tinnitus(ear-ringing),Hyperacusis,Insomnia,Tendon & muscle pain,feelings of death & doom,hallucinations,it goes on & on & on..... Its been over 2 years since I took the evil p...

Druginformer Identified Side Effects: Headache, Photophobia, Hyperacusis, Abdominal discomfort, Tinnitus, Walking disability, Eye disorder

Posted By Anonymous in askapatient.com on July 30, 2009 @ 12:00 am

Side Effects: Insomnea,Headaches,tinnitus(ear-ring)hyperacusi(sound sensitivity)Torn rotator cuff(shoulder)Plantar Fascias(feet)eye issue,stomach issues....the list goes on & on with Cipro....WAS A H...

Druginformer Identified Side Effects: Hyperacusis, Nausea, Nightmare, Tinnitus, Walking disability, Accidental poisoning, Central nervous system function test abnormal

Posted By Anonymous in askapatient.com on March 21, 2009 @ 12:00 am

Side Effects: Terrible drug - Wish I had never took it now - Capable of "delayed reactions" Can cripple you months/years down the line . Tinnitus , Hyperacusis,Insomnea ,nightmares, nausea ,CNS probl...



* 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.