How are Zicam adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Zicam, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Zicam is flagged as the suspect drug causing the adverse event.
What are the most common Zicam adverse events reported to the FDA?
Anosmia | 4235 (20.07%) |
Ageusia | 2919 (13.83%) |
Dysgeusia | 454 (2.15%) |
Nasal Discomfort | 341 (1.62%) |
Hyposmia | 340 (1.61%) |
Hypogeusia | 253 (1.2%) |
Burning Sensation | 247 (1.17%) |
Completed Suicide | 239 (1.13%) |
Drug Toxicity | 212 (1%) |
Overdose | 172 (.82%) |
Drug Abuse | 161 (.76%) |
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This graph shows the top adverse events submitted to the FDA for Zicam, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Zicam is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
What are the most common Zicam adverse events reported to the FDA?
Cranial Nerve Disorders | 4751 (22.51%) |
Neurological | 4564 (21.63%) |
Respiratory | 920 (4.36%) |
Medication Errors | 868 (4.11%) |
Psychiatric | 516 (2.45%) |
Cardiac Arrhythmias | 505 (2.39%) |
Suicidal And Self-injurious Behavio... | 391 (1.85%) |
Cardiac And Vascular Investigations | 378 (1.79%) |
Chemical Injury And Poisoning | 332 (1.57%) |
Upper Respiratory Tract Disorders | 300 (1.42%) |
Infections - Pathogen Unspecified | 290 (1.37%) |
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This graph shows the top categories of adverse events submitted to the FDA for Zicam, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Zicam is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
Why are people taking Zicam, according to those reporting adverse events to the FDA?
Nasopharyngitis | 1731 |
Drug Use For Unknown Indication | 387 |
Product Used For Unknown Indication | 335 |
Nasal Congestion | 328 |
Cough | 289 |
Upper Respiratory Tract Infection | 84 |
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Label | Labeler | Effective |
---|---|---|
Zicam | Matrixx Initiatives, Inc. | 21-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 21-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 28-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 28-DEC-09 |
Zicamcough Max | Matrixx Initiatives, Inc. | 28-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 28-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 28-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 28-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 28-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 29-DEC-09 |
Zicam | Matrixx Initiatives, Inc. | 29-DEC-09 |
Zicam Allergy Relief | Matrixx Initiatives, Inc. | 29-JUN-10 |
Zicamnaturals Cough Suppressant | Matrixx Initiatives, Inc. | 19-NOV-10 |
Zicam | Matrixx Initiatives, Inc. | 29-DEC-10 |
Zicamcold Remedy | Matrixx Initiatives, Inc. | 29-DEC-10 |
Zicam | Matrixx Initiatives, Inc. | 29-DEC-10 |
Zicam | Matrixx Initiatives, Inc. | 30-DEC-10 |
Zicamcold Remedy Zavors | Matrixx Initiatives, Inc. | 30-DEC-10 |
Zicam | Matrixx Initiatives, Inc. | 06-JAN-11 |
Zicam | Matrixx Initiatives, Inc. | 12-JAN-11 |
Zicam Naturals Cough Suppressant | Matrixx Initiatives, Inc. | 03-FEB-11 |
Zicam | Matrixx Initiatives, Inc. | 15-FEB-11 |
Zicam Cold Remedy Rapidmelts With Echinacea | Matrixx Initiatives, Inc. | 12-SEP-11 |
Zicamcold Remedy Rapidmelts Citrus | Matrixx Initiatives, Inc. | 20-SEP-11 |
Zicam Cold Remedy Ultra Rapidmelts | Matrixx Initiatives, Inc. | 07-OCT-11 |
Zicamcold Remedy Ultra Rapidmelts | Matrixx Initiatives, Inc. | 07-OCT-11 |
Zicam Ultra Cold Remedy | Matrixx Initiatives, Inc. | 08-JUN-12 |
Zicam Cold Remedy Rapidmelts | Matrixx Initiatives, Inc. | 09-JUL-12 |
Zicam Allergy Relief | Matrixx Initiatives, Inc. | 19-JUL-12 |
Zicam Cold Remedy Plus Mist | Matrixx Initiatives, Inc. | 20-JUL-12 |
Zicam Ultra Cold Remedy | Matrixx Initiatives, Inc. | 23-JUL-12 |
Zicam Naturals Cough Suppressant | Matrixx Initiatives, Inc. | 23-JUL-12 |
Zicam Ultra Cold Remedy Rapidmelts | Matrixx Initiatives, Inc. | 16-AUG-12 |
Zicam Ultra Cold Remedy Rapidmelts | Matrixx Initiatives, Inc. | 16-AUG-12 |
Zicam Cold Remedy Ultra Rapidmelts | Matrixx Initiatives, Inc. | 26-FEB-13 |
Zicam Cold Remedy Liqui-loz | Matrixx Initiatives, Inc. | 27-FEB-13 |
Zicam Cold Remedy Rapidmelts | Matrixx Initiatives, Inc. | 27-FEB-13 |
Zicam Cold Remedy Ultra Rapidmelts | Matrixx Initiatives, Inc. | 20-MAR-13 |
Zicam Cold Remedy Oral Mist | Matrixx Initiatives, Inc. | 29-MAR-13 |
Zicam Cold Remedy Oral Mist | Matrixx Initiatives, Inc. | 29-MAR-13 |
Zicam | Matrixx Initiatives, Inc. | 04-APR-13 |
Zicam Naturals Cough Suppressant | Matrixx Initiatives, Inc. | 04-APR-13 |
Zicam Allergy Relief | Matrixx Initiatives, Inc. | 04-APR-13 |
Zicam | Matrixx Initiatives, Inc. | 04-APR-13 |
What Zicam safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Zicam. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.
DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.
DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.
Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.
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