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ZITHROMAX

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Zithromax Adverse Events Reported to the FDA Over Time

How are Zithromax adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Zithromax, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Zithromax is flagged as the suspect drug causing the adverse event.

Most Common Zithromax Adverse Events Reported to the FDA

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

Diarrhoea
240 (1.67%)
Drug Ineffective
221 (1.54%)
Vomiting
210 (1.46%)
Nausea
208 (1.45%)
Rash
176 (1.23%)
Pyrexia
175 (1.22%)
Dyspnoea
170 (1.19%)
Abdominal Pain
135 (.94%)
Hypersensitivity
134 (.93%)
Headache
132 (.92%)
Urticaria
129 (.9%)
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Drug Hypersensitivity
119 (.83%)
Drug Interaction
117 (.82%)
Pneumonia
114 (.79%)
Malaise
113 (.79%)
Abdominal Pain Upper
104 (.73%)
Anxiety
99 (.69%)
Pruritus
98 (.68%)
Weight Decreased
92 (.64%)
Stevens-johnson Syndrome
91 (.63%)
Loss Of Consciousness
89 (.62%)
Fatigue
85 (.59%)
Dizziness
84 (.59%)
Deafness
82 (.57%)
Cough
80 (.56%)
Asthenia
79 (.55%)
Pain
78 (.54%)
Anosmia
76 (.53%)
Rhabdomyolysis
76 (.53%)
Tinnitus
76 (.53%)
Condition Aggravated
75 (.52%)
Ageusia
70 (.49%)
Feeling Abnormal
70 (.49%)
Alanine Aminotransferase Increased
65 (.45%)
Aspartate Aminotransferase Increase...
65 (.45%)
Convulsion
64 (.45%)
Erythema
61 (.43%)
Insomnia
61 (.43%)
Medication Error
56 (.39%)
Tremor
55 (.38%)
Chest Pain
54 (.38%)
Bronchitis
52 (.36%)
Cardiac Arrest
52 (.36%)
Liver Disorder
51 (.36%)
Oedema Peripheral
51 (.36%)
Anaphylactic Shock
50 (.35%)
Shock
50 (.35%)
Drug Eruption
49 (.34%)
Abdominal Discomfort
48 (.33%)
C-reactive Protein Increased
48 (.33%)
Dysgeusia
48 (.33%)
Hypoaesthesia
47 (.33%)
Chills
45 (.31%)
Palpitations
45 (.31%)
Blood Pressure Decreased
44 (.31%)
Electrocardiogram Qt Prolonged
43 (.3%)
Asthma
42 (.29%)
Heart Rate Increased
42 (.29%)
Sinusitis
42 (.29%)
Dysphagia
41 (.29%)
Hepatic Function Abnormal
41 (.29%)
Interstitial Lung Disease
41 (.29%)
Pancytopenia
41 (.29%)
Tachycardia
41 (.29%)
Decreased Appetite
40 (.28%)
Dehydration
40 (.28%)
Haematochezia
40 (.28%)
Somnolence
39 (.27%)
Swelling Face
39 (.27%)
Viral Infection
38 (.26%)
Drug Exposure During Pregnancy
37 (.26%)
Myalgia
36 (.25%)
Anorexia
35 (.24%)
Death
35 (.24%)
Nasopharyngitis
35 (.24%)
Pallor
35 (.24%)
Rash Generalised
35 (.24%)
Renal Failure
35 (.24%)
Swelling
35 (.24%)
Arthralgia
34 (.24%)
Confusional State
34 (.24%)
Renal Impairment
34 (.24%)
Blood Pressure Increased
33 (.23%)
Hallucination
33 (.23%)
Infection
33 (.23%)
Blister
32 (.22%)
Chromaturia
32 (.22%)
Conversion Disorder
32 (.22%)
Delirium
32 (.22%)
Paraesthesia
32 (.22%)
Depression
31 (.22%)
Pain In Extremity
31 (.22%)
Blood Alkaline Phosphatase Increase...
30 (.21%)
Blood Creatinine Increased
30 (.21%)
Blood Glucose Increased
30 (.21%)
Jaundice
30 (.21%)
Respiratory Arrest
30 (.21%)
Anaemia
29 (.2%)
Eating Disorder
29 (.2%)
Muscle Spasms
29 (.2%)
Stomatitis
29 (.2%)

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This graph shows the top adverse events submitted to the FDA for Zithromax, 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 Zithromax 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 Zithromax

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

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This graph shows the top categories of adverse events submitted to the FDA for Zithromax, 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 Zithromax 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 Zithromax According to Those Reporting Adverse Events

Why are people taking Zithromax, according to those reporting adverse events to the FDA?

Bronchitis
453
Pneumonia
336
Sinusitis
318
Upper Respiratory Tract Infection
231
Ill-defined Disorder
227
Drug Use For Unknown Indication
174
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Infection
158
Pharyngitis
146
Nasopharyngitis
146
Product Used For Unknown Indication
131
Pyrexia
131
Cough
108
Prophylaxis
102
Infection Prophylaxis
96
Upper Respiratory Tract Inflammatio...
86
Respiratory Tract Infection
86
Ear Infection
84
Opportunistic Infection Prophylaxis
82
Antibiotic Prophylaxis
73
Pharyngolaryngeal Pain
63
Mycobacterium Avium Complex Infecti...
60
Tonsillitis
50
Pharyngitis Streptococcal
47
Pneumonia Mycoplasmal
42
Chlamydial Infection
41
Oropharyngeal Pain
41
Bacterial Infection
36
Otitis Media
33
Acne
33
Influenza
32
Trachoma
28
Lyme Disease
27
Antibiotic Therapy
27
Bronchitis Acute
25
Sinobronchitis
25
Viral Infection
25
Urinary Tract Infection
22
Lung Infection
22
Lower Respiratory Tract Infection
21
Bronchopneumonia
21
Mycoplasma Infection
20
Respiratory Disorder
20
Chronic Obstructive Pulmonary Disea...
19
Acute Tonsillitis
18
Streptococcal Infection
16
Periodontitis
16
Asthma
16
Dyspnoea
16
Influenza Like Illness
14
Lung Disorder
13
Pertussis
12

Drug Labels

LabelLabelerEffective
ZithromaxPD-Rx Pharmaceuticals, Inc.11-MAR-11
ZithromaxREMEDYREPACK INC. 12-MAR-13
ZithromaxPfizer Laboratories Div Pfizer Inc03-APR-13
ZithromaxPfizer Laboratories Div Pfizer Inc03-APR-13
ZithromaxREMEDYREPACK INC. 04-APR-13
ZithromaxPfizer Laboratories Div Pfizer Inc05-APR-13

Zithromax Case Reports

What Zithromax 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 Zithromax. 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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