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ALEVE D SINUS AND COLD

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Aleve D Sinus And Cold Adverse Events Reported to the FDA Over Time

How are Aleve D Sinus And Cold adverse event reports trending over time?

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

Most Common Aleve D Sinus And Cold Adverse Events Reported to the FDA

What are the most common Aleve D Sinus And Cold adverse events reported to the FDA?

Insomnia
35 (7.8%)
Nasopharyngitis
28 (6.24%)
No Adverse Event
24 (5.35%)
Headache
18 (4.01%)
Sinus Headache
14 (3.12%)
Fatigue
13 (2.9%)
Dizziness
12 (2.67%)
Sinus Congestion
11 (2.45%)
Feeling Abnormal
10 (2.23%)
Hyperhidrosis
10 (2.23%)
Abdominal Pain Upper
9 (2%)
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Feeling Jittery
9 (2%)
Palpitations
9 (2%)
Nausea
8 (1.78%)
Pruritus
8 (1.78%)
Drug Screen Positive
6 (1.34%)
Dyspnoea
6 (1.34%)
Nasal Congestion
6 (1.34%)
Rhinorrhoea
6 (1.34%)
Vomiting
6 (1.34%)
Anxiety
5 (1.11%)
Hypersensitivity
5 (1.11%)
Nervousness
5 (1.11%)
Sinus Disorder
5 (1.11%)
Drug Ineffective
4 (.89%)
Dyspepsia
4 (.89%)
Hot Flush
4 (.89%)
Malaise
4 (.89%)
Somnolence
4 (.89%)
Unevaluable Event
4 (.89%)
Urticaria
4 (.89%)
Abdominal Discomfort
3 (.67%)
Asthenia
3 (.67%)
Blister
3 (.67%)
Chills
3 (.67%)
Feeling Cold
3 (.67%)
Hypotension
3 (.67%)
Mental Impairment
3 (.67%)
Middle Insomnia
3 (.67%)
Pain In Extremity
3 (.67%)
Pollakiuria
3 (.67%)
Psychomotor Hyperactivity
3 (.67%)
Pyrexia
3 (.67%)
Throat Irritation
3 (.67%)
Urine Flow Decreased
3 (.67%)
Abdominal Distension
2 (.45%)
Abdominal Pain
2 (.45%)
Anorexia
2 (.45%)
Constipation
2 (.45%)
Cough
2 (.45%)
Disturbance In Attention
2 (.45%)
Drug Effect Decreased
2 (.45%)
Dry Mouth
2 (.45%)
Dry Throat
2 (.45%)
Dysuria
2 (.45%)
Erythema
2 (.45%)
Euphoric Mood
2 (.45%)
Hypoaesthesia
2 (.45%)
Initial Insomnia
2 (.45%)
Irritable Bowel Syndrome
2 (.45%)
Migraine
2 (.45%)
Poor Quality Sleep
2 (.45%)
Pruritus Generalised
2 (.45%)
Rash
2 (.45%)
Rhinalgia
2 (.45%)
Sneezing
2 (.45%)
Swelling Face
2 (.45%)
Swollen Tongue
2 (.45%)
Wheezing
2 (.45%)
Abnormal Sensation In Eye
1 (.22%)
Adverse Event
1 (.22%)
Ageusia
1 (.22%)
Agitation
1 (.22%)
Anosmia
1 (.22%)
Aphagia
1 (.22%)
Back Pain
1 (.22%)
Balance Disorder
1 (.22%)
Confusional State
1 (.22%)
Contusion
1 (.22%)
Convulsion
1 (.22%)
Depression
1 (.22%)
Diarrhoea
1 (.22%)
Drug Screen False Positive
1 (.22%)
Dysarthria
1 (.22%)
Dysgeusia
1 (.22%)
Dysphonia
1 (.22%)
Erectile Dysfunction
1 (.22%)
Expired Drug Administered
1 (.22%)
Faecal Incontinence
1 (.22%)
Fall
1 (.22%)
Feeling Hot
1 (.22%)
Flushing
1 (.22%)
Formication
1 (.22%)
Gait Disturbance
1 (.22%)
Groin Pain
1 (.22%)
Haemoptysis
1 (.22%)
Head Injury
1 (.22%)
Heart Rate Decreased
1 (.22%)
Heart Rate Increased
1 (.22%)
Hypertension
1 (.22%)
Incorrect Dose Administered
1 (.22%)

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This graph shows the top adverse events submitted to the FDA for Aleve D Sinus And Cold, 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 Aleve D Sinus And Cold 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 Aleve D Sinus And Cold

What are the most common Aleve D Sinus And Cold adverse events reported to the FDA?

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

Why are people taking Aleve D Sinus And Cold, according to those reporting adverse events to the FDA?

Nasopharyngitis
94
Sinus Headache
30
Drug Use For Unknown Indication
21
Nasal Congestion
16
Product Used For Unknown Indication
13
Sinus Disorder
9
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Sinus Congestion
8
Headache
5
Sinusitis
4
Pain
2
Analgesic Therapy
2
Ear Pain
1
Migraine
1
Influenza
1
Seasonal Allergy
1
Multiple Allergies
1
Hypersensitivity
1
Respiratory Tract Congestion
1
Influenza Like Illness
1
Chronic Obstructive Pulmonary Disea...
1

Aleve D Sinus And Cold Case Reports

What Aleve D Sinus And Cold 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 Aleve D Sinus And Cold. 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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