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KLACID

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Klacid Adverse Events Reported to the FDA Over Time

How are Klacid adverse event reports trending over time?

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

Most Common Klacid Adverse Events Reported to the FDA

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

Dyspnoea
65 (2.18%)
Drug Interaction
50 (1.68%)
Pruritus
40 (1.34%)
Nausea
38 (1.27%)
Pyrexia
38 (1.27%)
Urticaria
37 (1.24%)
Suicide Attempt
33 (1.11%)
Vomiting
29 (.97%)
Completed Suicide
28 (.94%)
Hallucination
24 (.8%)
Erythema
23 (.77%)
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Rash
23 (.77%)
Renal Failure Acute
23 (.77%)
Confusional State
22 (.74%)
Headache
22 (.74%)
Respiratory Failure
21 (.7%)
Electrocardiogram Qt Prolonged
20 (.67%)
International Normalised Ratio Incr...
19 (.64%)
Abdominal Pain
18 (.6%)
Diarrhoea
18 (.6%)
Pain In Extremity
18 (.6%)
Asthenia
17 (.57%)
Cholestasis
17 (.57%)
General Physical Health Deteriorati...
17 (.57%)
Myalgia
17 (.57%)
Pneumonia
17 (.57%)
Rash Maculo-papular
17 (.57%)
Drug Level Increased
16 (.54%)
Hypersensitivity
16 (.54%)
Jaundice
16 (.54%)
Abdominal Pain Upper
15 (.5%)
Fatigue
15 (.5%)
Insomnia
15 (.5%)
Malaise
15 (.5%)
Rhabdomyolysis
15 (.5%)
Hepatitis Acute
14 (.47%)
Multi-organ Failure
14 (.47%)
Sepsis
14 (.47%)
Sleep Disorder
14 (.47%)
Agitation
13 (.44%)
Anaemia
13 (.44%)
C-reactive Protein Increased
13 (.44%)
Cardiac Failure
13 (.44%)
Dermatitis Allergic
13 (.44%)
Dizziness
13 (.44%)
Drug Ineffective
13 (.44%)
Ventricular Fibrillation
13 (.44%)
Condition Aggravated
12 (.4%)
Drug Administration Error
12 (.4%)
Face Oedema
12 (.4%)
Fall
12 (.4%)
Tremor
12 (.4%)
Aggression
11 (.37%)
Blood Creatinine Increased
11 (.37%)
Dehydration
11 (.37%)
Delirium
11 (.37%)
Eyelid Oedema
11 (.37%)
Hepatic Enzyme Increased
11 (.37%)
Hepatomegaly
11 (.37%)
Vasculitis
11 (.37%)
Aphthous Stomatitis
10 (.34%)
Arthralgia
10 (.34%)
Gait Disturbance
10 (.34%)
Hepatic Steatosis
10 (.34%)
Hypertension
10 (.34%)
Muscular Weakness
10 (.34%)
Pharyngeal Oedema
10 (.34%)
Stevens-johnson Syndrome
10 (.34%)
Swollen Tongue
10 (.34%)
Tachycardia
10 (.34%)
Cough
9 (.3%)
Extravasation
9 (.3%)
Injection Site Erythema
9 (.3%)
Overdose
9 (.3%)
Pallor
9 (.3%)
Sensory Loss
9 (.3%)
Tension
9 (.3%)
Alanine Aminotransferase Increased
8 (.27%)
Angioedema
8 (.27%)
Arm Amputation
8 (.27%)
Blister
8 (.27%)
Blood Creatine Phosphokinase Increa...
8 (.27%)
Circulatory Collapse
8 (.27%)
Clostridium Colitis
8 (.27%)
Conjunctivitis
8 (.27%)
Constipation
8 (.27%)
Convulsion
8 (.27%)
Feeling Hot
8 (.27%)
Grand Mal Convulsion
8 (.27%)
Haematoma
8 (.27%)
Laryngeal Oedema
8 (.27%)
Long Qt Syndrome
8 (.27%)
Pleural Effusion
8 (.27%)
Weight Decreased
8 (.27%)
Wheezing
8 (.27%)
Aspartate Aminotransferase Increase...
7 (.23%)
Back Pain
7 (.23%)
Bradycardia
7 (.23%)
Cardiac Arrest
7 (.23%)
Delusional Disorder, Unspecified Ty...
7 (.23%)
Drug Exposure During Pregnancy
7 (.23%)

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

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

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

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

Drug Use For Unknown Indication
113
Pneumonia
111
Helicobacter Infection
50
Bronchitis
47
Lower Respiratory Tract Infection
38
Product Used For Unknown Indication
33
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Pyrexia
28
Bronchopneumonia
25
Infection
24
Suicide Attempt
21
Respiratory Tract Infection
16
Sinusitis
15
Helicobacter Gastritis
13
Tonsillitis
12
Tooth Abscess
12
Upper Respiratory Tract Infection
12
Mycobacterium Avium Complex Infecti...
11
Pneumonia Primary Atypical
11
Pneumonia Bacterial
10
Gastritis
10
Lung Infection
10
Duodenal Ulcer
9
Chronic Obstructive Pulmonary Disea...
8
Cough
7
Influenza
7
Bronchitis Acute
7
Pharyngitis
6
Tracheitis
6
Nasopharyngitis
6
Oropharyngeal Pain
6
Duodenitis
6
Gastric Ulcer
6
Drug Exposure During Pregnancy
6
Atypical Mycobacterial Infection
5
Paronychia
5
Ear Infection
5
Depression
5
Lobar Pneumonia
4
Dyspepsia
4
Acute Tonsillitis
4
Odynophagia
4
Acute Sinusitis
4
Bronchitis Chronic
3
Lung Infiltration
3
Viral Infection
3
Cellulitis
3
Otitis Media
3
Infection Prophylaxis
3
Bacterial Infection
3
Abscess
3
Pneumonia Mycoplasmal
3

Klacid Case Reports

What Klacid 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 Klacid. 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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