Drug Safety Information for FENTANYL CITRATE AND DROPERIDOL (Droperidol; fentanyl citrate)

Adverse Drug Reactions for FENTANYL CITRATE AND DROPERIDOL* (Droperidol; fentanyl citrate)

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 FENTANYL CITRATE AND DROPERIDOL
(reported in FDA Medwatch/FAERS Reports)

  Side Effect # of FDA Reports
1Anaemia4
2Hypersensitivity3
3Eosinophilia3
4Asthma3
5Asthenia3
6Nausea3
7Malaise3
8Blood creatinine increased3
9Lipase increased3
10Cytolytic hepatitis2
11Dyspnoea2
12Dizziness2
13Hyponatraemia2
14Urticaria2
15Vomiting2
16Arthralgia2
17Muscle spasms2
18Tremor2
19Atrial fibrillation1
20Lipodystrophy acquired1

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

Top 10 Reasons for Taking FENTANYL CITRATE AND DROPERIDOL
(associated with FDA Medwatch/FAERS Reports)

Reason # of FDA Reports
1Asthma24
2Product used for unknown indication13
3Chronic obstructive pulmonary disease7
4Bronchitis chronic4
5Lower respiratory tract infection2

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


Types of Adverse Events for FENTANYL CITRATE AND DROPERIDOL

Total Reports Filed with FDA: 110


Number of FDA Adverse Event Reports by Patient Age for FENTANYL CITRATE AND DROPERIDOL

Total Reports Filed with FDA: 110*


* Reports for drugs with the same active ingredients have been aggregated in this analysis: Droperidol; fentanyl citrate (Innovar)

Charts are based on 110 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 FENTANYL CITRATE AND DROPERIDOL 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.

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