Drug Safety Information for NYSTATIN AND TRIAMCINOLONE ACETONIDE (Nystatin; triamcinolone acetonide)

Adverse Drug Reactions for NYSTATIN AND TRIAMCINOLONE ACETONIDE* (Nystatin; triamcinolone acetonide)

These charts and graphs are based on reports received through the FDA Adverse Event Reporting System (FAERS) program (see below).

Top 20 Adverse Effects Associated with NYSTATIN AND TRIAMCINOLONE ACETONIDE
(reported in FDA Medwatch/FAERS Reports)

  Side Effect # of FDA Reports
1Nausea8
2Arthralgia7
3Drug ineffective*6
4Pain*6
5Malaise5
6Vomiting5
7Fatigue5
8Pain in extremity5
9Anxiety4
10Urinary tract infection4
11Cellulitis4
12Asthenia4
13Convulsion4
14Pruritus4
15Deep vein thrombosis4
16Dizziness3
17Pancytopenia3
18Dry mouth3
19Cardiac disorder3
20Renal failure3

* This side effect also appears in "Top 10 Side Effects of NYSTATIN AND TRIAMCINOLONE ACETONIDE " in the drug's Review Summary based on AskaPatient reviews.

Top 10 Reasons for Taking NYSTATIN AND TRIAMCINOLONE ACETONIDE
(associated with FDA Medwatch/FAERS Reports)

Reason # of FDA Reports
1Product used for unknown indication27
2Dermatitis diaper17
3Oropharyngeal pain10
4Lip injury9
5Rash4
6Heat rash4
7Pruritus3
8Rash pruritic3
9Vulvovaginal mycotic infection*2
10Fungal infection*2

*Also a top-10 reason in AskaPatient Review Summary.


Types of Adverse Events for NYSTATIN AND TRIAMCINOLONE ACETONIDE

Total Reports Filed with FDA: 461


Number of FDA Adverse Event Reports by Patient Age for NYSTATIN AND TRIAMCINOLONE ACETONIDE

Total Reports Filed with FDA: 461*


* Reports for drugs with the same active ingredients have been aggregated in this analysis: Nystatin; triamcinolone acetonide (Mytrex f, Myco-triacet ii, Mykacet, Mycolog-ii)

Charts are based on 461 reports filed with the FDA between 2004 and June 2015.

Adverse Event Reports are submitted to the FDA by pharmaceutical companies (mandatory reporting is required by manufacturers, distributors, or importers), health care providers such as doctors (voluntary reporting), and by patients themselves (voluntary reporting). More Information on FDA MedWatch (FDA Safety Information and Adverse Event Reporting Program)Voluntary reporting takes place under the FDA's MedWatch program, where health care professionals and consumers submit reports to FDA when they find a problem with a drug, medical device, biologic, or other FDA-regulated product. An adverse event is any undesirable experience or extreme side effect associated with the use of a medical product. Adverse events include: death, life threatening event, hospitalization, disability or permanent damage, congenital anomaly or birth defect, medical product use requiring a surgical or other intervention, or other serious medical situation believed to be caused by the drug.

Click to go back to search results and NYSTATIN AND TRIAMCINOLONE ACETONIDE Reviews and Review Summary .

Analytics of FDA Adverse Event Reports Provided by Druginformer.com. FDA Drug Safety Information, including safety-related labeling updates, required post-approval safety studies, risk evaluation management strategies (REMS), alerts, and recalls are compiled by AskaPatient.com from the U.S. Food and Drug Administration.

Visit   DrugInformer.com more on NYSTATIN AND TRIAMCINOLONE ACETONIDE's side effects.