Drug Safety Information for AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER (Moxifloxacin hydrochloride)
Safety-related Labeling Changes for AVELOX (MOXIFLOXACIN HYDROCHLORIDE) Rx Drug: FDA Link
Risk of mitral and aortic regurgitation Evaluating
Safety-related Labeling Changes for VIGAMOX (MOXIFLOXACIN HYDROCHLORIDE) Rx Drug: FDA Link
Adverse Drug Reactions for AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER* (Moxifloxacin hydrochloride)
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 AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER
(reported in FDA Medwatch/FAERS Reports)
|Side Effect||# of FDA Reports|
|18||Pain in extremity||550|
* This side effect also appears in "Top 10 Side Effects of AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER " in the drug's Review Summary based on AskaPatient reviews.
Top 10 Reasons for Taking AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER
(associated with FDA Medwatch/FAERS Reports)
|Reason||# of FDA Reports|
|1||Product used for unknown indication||10478|
|5||Upper respiratory tract infection*||1305|
|7||Respiratory tract infection*||1047|
|10||Urinary tract infection*||428|
*Also a top-10 reason in AskaPatient Review Summary.
Types of Adverse Events for AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER
Total Reports Filed with FDA: 83631
Number of FDA Adverse Event Reports by Patient Age for AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER
Total Reports Filed with FDA: 83631*
* Reports for drugs with the same active ingredients have been aggregated in this analysis: Moxifloxacin hydrochloride (Moxifloxacin, Moxifloxacin hcl, Avelox abc pack, Actira, Proflox, Octegra, Izilox, Avelox, Vigamox, Moxeza)
Charts are based on 83631 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.
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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.