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ALLEGRA D

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Allegra D Adverse Events Reported to the FDA Over Time

How are Allegra D adverse event reports trending over time?

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

Most Common Allegra D Adverse Events Reported to the FDA

What are the most common Allegra D adverse events reported to the FDA?

Completed Suicide
217 (1.77%)
Drug Ineffective
211 (1.72%)
Dizziness
170 (1.38%)
Drug Toxicity
160 (1.3%)
Loss Of Consciousness
154 (1.25%)
Vomiting
151 (1.23%)
Dyspnoea
143 (1.16%)
Malaise
141 (1.15%)
Nausea
134 (1.09%)
Insomnia
113 (.92%)
Headache
112 (.91%)
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Convulsion
106 (.86%)
Death
98 (.8%)
Rash
93 (.76%)
Overdose
91 (.74%)
Alanine Aminotransferase Increased
87 (.71%)
Palpitations
86 (.7%)
Hepatic Function Abnormal
85 (.69%)
Hypersensitivity
85 (.69%)
Urticaria
85 (.69%)
Aspartate Aminotransferase Increase...
83 (.68%)
Pruritus
81 (.66%)
Somnolence
80 (.65%)
Fatigue
77 (.63%)
Feeling Abnormal
76 (.62%)
Heart Rate Increased
76 (.62%)
Jaundice
75 (.61%)
Liver Disorder
74 (.6%)
Tachycardia
74 (.6%)
Cardiac Arrest
73 (.59%)
Drug Interaction
70 (.57%)
Hypertension
69 (.56%)
Asthenia
68 (.55%)
Pyrexia
68 (.55%)
Chest Pain
67 (.54%)
Hallucination
64 (.52%)
Hypoaesthesia
59 (.48%)
Cardio-respiratory Arrest
58 (.47%)
Condition Aggravated
58 (.47%)
Diarrhoea
57 (.46%)
Fall
56 (.46%)
Abdominal Pain Upper
55 (.45%)
Anxiety
54 (.44%)
Blood Pressure Increased
54 (.44%)
Medication Residue
54 (.44%)
Abdominal Pain
52 (.42%)
Swelling Face
51 (.41%)
Syncope
50 (.41%)
Respiratory Arrest
49 (.4%)
Tremor
48 (.39%)
Hypotension
46 (.37%)
Medication Error
46 (.37%)
Chest Discomfort
45 (.37%)
Pneumonia
44 (.36%)
Platelet Count Decreased
43 (.35%)
Multiple Drug Overdose
42 (.34%)
Paraesthesia
42 (.34%)
Drug Hypersensitivity
41 (.33%)
Dry Mouth
39 (.32%)
Electrocardiogram Qt Prolonged
39 (.32%)
Erythema
39 (.32%)
Nervousness
39 (.32%)
Oedema Peripheral
39 (.32%)
Pain
39 (.32%)
Cerebrovascular Accident
38 (.31%)
Drug Exposure During Pregnancy
38 (.31%)
Agitation
37 (.3%)
Intentional Overdose
37 (.3%)
Sudden Infant Death Syndrome
37 (.3%)
Weight Decreased
37 (.3%)
Decreased Appetite
36 (.29%)
Depression
36 (.29%)
Muscle Spasms
36 (.29%)
Myocardial Infarction
36 (.29%)
Atrial Fibrillation
35 (.28%)
Cough
35 (.28%)
Renal Impairment
35 (.28%)
Dysgeusia
34 (.28%)
Arrhythmia
33 (.27%)
Back Pain
33 (.27%)
Confusional State
33 (.27%)
Hyperhidrosis
33 (.27%)
Urinary Retention
33 (.27%)
Abdominal Discomfort
32 (.26%)
Blood Alkaline Phosphatase Increase...
32 (.26%)
Incorrect Dose Administered
32 (.26%)
Therapeutic Response Unexpected Wit...
32 (.26%)
Intentional Drug Misuse
31 (.25%)
Angioedema
30 (.24%)
Accidental Drug Intake By Child
29 (.24%)
Anaemia
29 (.24%)
Disorientation
29 (.24%)
Gamma-glutamyltransferase Increased
29 (.24%)
Off Label Use
29 (.24%)
Product Quality Issue
29 (.24%)
Vision Blurred
29 (.24%)
Abnormal Behaviour
28 (.23%)
Asthma
28 (.23%)
Blood Bilirubin Increased
28 (.23%)
Dysphagia
28 (.23%)
Flushing
27 (.22%)

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

What are the most common Allegra D adverse events reported to the FDA?

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

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

Hypersensitivity
1784
Drug Use For Unknown Indication
1068
Product Used For Unknown Indication
834
Seasonal Allergy
710
Multiple Allergies
685
Rhinitis Allergic
374
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Urticaria
181
Nasopharyngitis
164
Pruritus
150
Sinus Disorder
126
Asthma
123
Nasal Congestion
111
Sinusitis
108
Rhinitis
105
Rash
80
Prophylaxis
76
Premedication
65
Sinus Congestion
61
Cough
60
Eczema
49
Upper Respiratory Tract Infection
41
Allergic Sinusitis
38
Suicide Attempt
35
Sinus Headache
35
Ill-defined Disorder
34
Antiallergic Therapy
33
Chronic Sinusitis
27
Influenza
26
Urticaria Chronic
24
Headache
22
Dermatitis
21
Dermatitis Atopic
20
Dermatitis Allergic
19
Rhinitis Seasonal
18
Rhinorrhoea
17
Accidental Exposure
17
Nasal Decongestion Therapy
16
Pain
15
Diarrhoea
14
Postnasal Drip
13
Pharyngitis
12
Pyrexia
12
Conjunctivitis Allergic
12
Intentional Overdose
11
Pruritus Generalised
11
Bronchitis
10
Acute Sinusitis
10
Drug Eruption
10
Palmar-plantar Erythrodysaesthesia ...
10
Chronic Obstructive Pulmonary Disea...
9
Dyspnoea
9

Drug Labels

LabelLabelerEffective
AllegraSanofi-Synthelabo Limited15-DEC-08
Allegra-dbryant ranch prepack04-MAR-09
Allegra D-12 Hoursanofi-aventis U.S. LLC08-DEC-09
Allegra D-12 HourPhysicians Total Care, Inc.08-DEC-09
Allegra--d 24 Hoursanofi-aventis U.S. LLC11-DEC-09
Allegra-d 24 Hour STAT RX USA LLC15-DEC-09
Childrens Allegra AllergyChattem, Inc.02-JUL-11
Allegra D 12 Hour Allergy And CongestionRebel Distributors Corp20-JUL-11
Allegra D 12 Hour Allergy And CongestionChattem, Inc.18-AUG-11
Allegra--d 24 Hour Allergy And CongestionChattem, Inc.18-AUG-11
Allegrasanofi-aventis U.S. LLC21-MAR-12
Childrens Allegra AllergyChattem, Inc.05-APR-12
Allegra AllergyChattem, Inc.05-APR-12
Childrens Allegra AllergyChattem, Inc.30-APR-12
Allegra--d 24 HourPhysicians Total Care, Inc.25-SEP-12
Allegra Cooling Relief Anti-itchChattem, Inc.29-APR-13
Allegra Intensive Relief Anti-itchChattem, Inc.29-APR-13

Allegra D Case Reports

What Allegra D 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 Allegra D. 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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