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Zicam Adverse Events Reported to the FDA Over Time

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.

Most Common Zicam Adverse Events Reported to the FDA

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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Parosmia
156 (.74%)
Intentional Drug Misuse
136 (.64%)
Intentional Overdose
129 (.61%)
Drug Dependence
123 (.58%)
Dyspnoea
120 (.57%)
Cardiac Arrest
112 (.53%)
Headache
112 (.53%)
Drug Interaction
107 (.51%)
Vomiting
103 (.49%)
Respiratory Arrest
100 (.47%)
Blood Pressure Increased
99 (.47%)
Convulsion
95 (.45%)
Multiple Injuries
94 (.45%)
Agitation
89 (.42%)
Cardio-respiratory Arrest
86 (.41%)
Heart Rate Increased
86 (.41%)
Pain
78 (.37%)
Dysarthria
77 (.36%)
Drug Ineffective
75 (.36%)
Loss Of Consciousness
75 (.36%)
Nasal Congestion
74 (.35%)
Serotonin Syndrome
74 (.35%)
Suicide Attempt
74 (.35%)
Death
71 (.34%)
Incorrect Dose Administered
70 (.33%)
Rhinalgia
69 (.33%)
Toxic Anterior Segment Syndrome
69 (.33%)
Dizziness
68 (.32%)
Nausea
67 (.32%)
Psychotic Disorder
67 (.32%)
Aggression
66 (.31%)
Medication Error
64 (.3%)
Product Quality Issue
64 (.3%)
Confusional State
62 (.29%)
Condition Aggravated
61 (.29%)
Depression
61 (.29%)
Incorrect Drug Administration Durat...
60 (.28%)
Palpitations
60 (.28%)
Disturbance In Attention
59 (.28%)
Hypertension
59 (.28%)
Accidental Overdose
58 (.27%)
Abnormal Behaviour
56 (.27%)
Anxiety
56 (.27%)
Pyrexia
56 (.27%)
Cardiac Disorder
55 (.26%)
Hypersensitivity
54 (.26%)
Tachycardia
53 (.25%)
Suicidal Ideation
52 (.25%)
Epistaxis
50 (.24%)
Flat Affect
50 (.24%)
Insomnia
50 (.24%)
Lacrimation Increased
50 (.24%)
Somnolence
50 (.24%)
Atrioventricular Block
48 (.23%)
Ventricular Extrasystoles
48 (.23%)
Heart Rate Irregular
47 (.22%)
Mydriasis
47 (.22%)
Hallucination
46 (.22%)
Pulmonary Oedema
44 (.21%)
Rhabdomyolysis
44 (.21%)
Rhinorrhoea
44 (.21%)
Tangentiality
44 (.21%)
Lethargy
42 (.2%)
Tremor
42 (.2%)
Multiple Drug Overdose
41 (.19%)
Sinus Disorder
41 (.19%)
Blood Creatine Phosphokinase Increa...
40 (.19%)
Extrasystoles
40 (.19%)
Feeling Abnormal
40 (.19%)
Hypotension
40 (.19%)
Malaise
40 (.19%)
Poisoning
40 (.19%)
Wrong Drug Administered
40 (.19%)
Cardiotoxicity
39 (.18%)
Disorientation
38 (.18%)
Drug Exposure During Pregnancy
38 (.18%)
Hallucination, Visual
38 (.18%)
Nasopharyngitis
38 (.18%)
Endophthalmitis
37 (.18%)
Fall
37 (.18%)
Pneumonia
36 (.17%)
Hyperhidrosis
35 (.17%)
Inflammation
34 (.16%)
Multiple Drug Overdose Intentional
34 (.16%)
Chest Pain
33 (.16%)
Coma
33 (.16%)
Drug Abuser
33 (.16%)
Drug Hypersensitivity
33 (.16%)
Euphoric Mood
33 (.16%)
Alcohol Problem
32 (.15%)

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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.

Adverse Event Categories for Zicam

What are the most common Zicam adverse events reported to the FDA?

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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.

Common Uses of Zicam According to Those Reporting Adverse Events

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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Preoperative Care
83
Influenza
80
Prophylaxis
78
Sinus Congestion
66
Hypersensitivity
62
Hypotension
61
Mydriasis
54
Suicide Attempt
54
Sinus Disorder
51
Sinusitis
45
Cataract Operation
42
Multiple Allergies
37
Drug Abuse
31
Rhinorrhoea
30
Seasonal Allergy
30
Ill-defined Disorder
29
Intentional Overdose
29
Influenza Like Illness
23
Oropharyngeal Pain
23
Anosmia
23
Pyrexia
22
Insomnia
21
Ophthalmological Examination
21
Dyspnoea
19
Off Label Use
18
Headache
17
Accidental Exposure
17
Bronchitis
16
Sinus Headache
15
Anaesthesia
14
Reversible Ischaemic Neurological D...
14
Blood Pressure Management
13
Malaise
13
Intentional Drug Misuse
13
Pharyngolaryngeal Pain
12
Drug Exposure During Pregnancy
11
Sleep Disorder
11
Antitussive Therapy
11
Pain
11
Respiratory Tract Infection
10
Viral Infection
10
Sneezing
10
Feeling Cold
9
Euphoric Mood
9
Upper Respiratory Tract Inflammatio...
8

Drug Labels

LabelLabelerEffective
ZicamMatrixx Initiatives, Inc.21-DEC-09
ZicamMatrixx Initiatives, Inc.21-DEC-09
ZicamMatrixx Initiatives, Inc.28-DEC-09
ZicamMatrixx Initiatives, Inc.28-DEC-09
Zicamcough MaxMatrixx Initiatives, Inc.28-DEC-09
ZicamMatrixx Initiatives, Inc.28-DEC-09
ZicamMatrixx Initiatives, Inc.28-DEC-09
ZicamMatrixx Initiatives, Inc.28-DEC-09
ZicamMatrixx Initiatives, Inc.28-DEC-09
ZicamMatrixx Initiatives, Inc.29-DEC-09
ZicamMatrixx Initiatives, Inc.29-DEC-09
Zicam Allergy ReliefMatrixx Initiatives, Inc.29-JUN-10
Zicamnaturals Cough SuppressantMatrixx Initiatives, Inc.19-NOV-10
ZicamMatrixx Initiatives, Inc.29-DEC-10
Zicamcold RemedyMatrixx Initiatives, Inc.29-DEC-10
ZicamMatrixx Initiatives, Inc.29-DEC-10
ZicamMatrixx Initiatives, Inc.30-DEC-10
Zicamcold Remedy ZavorsMatrixx Initiatives, Inc.30-DEC-10
ZicamMatrixx Initiatives, Inc.06-JAN-11
ZicamMatrixx Initiatives, Inc.12-JAN-11
Zicam Naturals Cough SuppressantMatrixx Initiatives, Inc.03-FEB-11
ZicamMatrixx Initiatives, Inc.15-FEB-11
Zicam Cold Remedy Rapidmelts With EchinaceaMatrixx Initiatives, Inc.12-SEP-11
Zicamcold Remedy Rapidmelts CitrusMatrixx Initiatives, Inc.20-SEP-11
Zicam Cold Remedy Ultra RapidmeltsMatrixx Initiatives, Inc.07-OCT-11
Zicamcold Remedy Ultra RapidmeltsMatrixx Initiatives, Inc.07-OCT-11
Zicam Ultra Cold RemedyMatrixx Initiatives, Inc.08-JUN-12
Zicam Cold Remedy RapidmeltsMatrixx Initiatives, Inc.09-JUL-12
Zicam Allergy ReliefMatrixx Initiatives, Inc.19-JUL-12
Zicam Cold Remedy Plus MistMatrixx Initiatives, Inc.20-JUL-12
Zicam Ultra Cold RemedyMatrixx Initiatives, Inc.23-JUL-12
Zicam Naturals Cough SuppressantMatrixx Initiatives, Inc.23-JUL-12
Zicam Ultra Cold Remedy RapidmeltsMatrixx Initiatives, Inc.16-AUG-12
Zicam Ultra Cold Remedy RapidmeltsMatrixx Initiatives, Inc.16-AUG-12
Zicam Cold Remedy Ultra RapidmeltsMatrixx Initiatives, Inc.26-FEB-13
Zicam Cold Remedy Liqui-lozMatrixx Initiatives, Inc.27-FEB-13
Zicam Cold Remedy RapidmeltsMatrixx Initiatives, Inc.27-FEB-13
Zicam Cold Remedy Ultra RapidmeltsMatrixx Initiatives, Inc.20-MAR-13
Zicam Cold Remedy Oral MistMatrixx Initiatives, Inc.29-MAR-13
Zicam Cold Remedy Oral MistMatrixx Initiatives, Inc.29-MAR-13
ZicamMatrixx Initiatives, Inc.04-APR-13
Zicam Naturals Cough SuppressantMatrixx Initiatives, Inc.04-APR-13
Zicam Allergy ReliefMatrixx Initiatives, Inc.04-APR-13
ZicamMatrixx Initiatives, Inc.04-APR-13

Zicam Case Reports

What Zicam safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

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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