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Sporanox

Ingredients: Itraconazole
Average User Review Score
* Based on 42 reviews from across the web.
Wikipedia

Itraconazole (R51211), invented in 1984, is a triazole antifungal agent prescribed to patients with fungal infections. The drug may be given orally or intravenously.

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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: Nausea, Abdominal discomfort, Hepatic function abnormal, Insomnia, Urine colour abnormal, Arthralgia, Headache, Menstruation irregular

Posted By Anonymous in askapatient.com on April 11, 2015 @ 12:00 am

Side Effects: Insomnia, nausea, headaches, joint pain, had no period at all this month, stomach pain, & really dark urine - which could mean liver problems (hopefully not) I'm stopping & ma...

Druginformer Identified Side Effects: Paraesthesia, Rash, Hypertension, Chills, Hepatic congestion

Posted By Anonymous in askapatient.com on December 8, 2014 @ 12:00 am

Side Effects: Took for 2 days got head chills, leg tingling, right ear felt congested, rash on leg and arm and chest elevated blood pressure sent me to er.Had to be put on steriods.Dont take this med...

Druginformer Identified Side Effects: Hypoaesthesia

Posted By Anonymous in askapatient.com on July 13, 2014 @ 12:00 am

Side Effects: Numbness in hands and feet

Druginformer Identified Side Effects: Oedema

Posted By Anonymous in askapatient.com on November 14, 2013 @ 12:00 am

Side Effects: Pitting edema of lower legs

Druginformer Identified Side Effects: Somnolence

Posted By Anonymous in askapatient.com on May 13, 2013 @ 12:00 am

Side Effects: possible fatigue looked well enough that I could remove bandage covering lesion after 2 mos. Every MD that looks at it says- yeah its good. Since it is still red and does no...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on April 15, 2013 @ 12:00 am

Side Effects: Do not know where to begin...Is my father who is taking it and has gotten CHF while on it, one of my biggest issues is that it has NOT helped the 19 lesions on his brain and the fact th...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on March 9, 2013 @ 12:00 am

Side Effects: none worried about possible side affects based primarily on what I read here at this site. So far, knock on wood, nothing. Inflamation was reduced within 5 days. big relief. T...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on February 17, 2013 @ 12:00 am

Side Effects: At first I couldn't keep it down so I started drinking coca cola 15 minutes before taking it. After a couple of weeks I realized that I could keep it dow n without coca cola so I stoppe...

Druginformer Identified Side Effects: Nausea, Food allergy, Death, Somnolence

Posted By Anonymous in askapatient.com on January 5, 2013 @ 12:00 am

Side Effects: Horrible floaters in eyes, stomach torn to bits, nausea, fatigue Since taking sporanox pulsed 400 mg a day for 7 days then 3 weeks off for 6 months I have never felt the same ...

Druginformer Identified Side Effects: Anxiety, Confusional state, Depression, Rash, Psychotic disorder

Posted By Anonymous in askapatient.com on November 16, 2012 @ 12:00 am

Side Effects: Within hours of taking this medication I began to feel confused, anxious and began to develop a rash on my stomach. I literally felt like something was happening to my brain. I only t...


* 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.