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COFFEE

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Coffee Adverse Events Reported to the FDA Over Time

How are Coffee adverse event reports trending over time?

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

Most Common Coffee Adverse Events Reported to the FDA

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

Abnormal Dreams
64 (1.38%)
Fatigue
63 (1.36%)
Insomnia
63 (1.36%)
Nausea
62 (1.34%)
Headache
61 (1.31%)
Heart Rate Increased
61 (1.31%)
Ill-defined Disorder
61 (1.31%)
Somnolence
61 (1.31%)
Weight Increased
60 (1.29%)
Back Pain
59 (1.27%)
Diarrhoea
59 (1.27%)
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Drug Ineffective
59 (1.27%)
Dyspnoea
59 (1.27%)
Irritability
59 (1.27%)
Memory Impairment
59 (1.27%)
Stress
59 (1.27%)
Tension
59 (1.27%)
Anxiety
58 (1.25%)
Arthropathy
58 (1.25%)
Blood Pressure Increased
58 (1.25%)
Influenza Like Illness
58 (1.25%)
Sleep Talking
58 (1.25%)
Somnambulism
58 (1.25%)
Urinary Tract Infection
58 (1.25%)
Viral Infection
58 (1.25%)
Vulvovaginal Burning Sensation
58 (1.25%)
Weight Decreased
58 (1.25%)
Abortion Spontaneous
57 (1.23%)
Bed Rest
57 (1.23%)
Mood Altered
57 (1.23%)
Thrombosis
57 (1.23%)
Sleep Disorder
56 (1.21%)
Abnormal Behaviour
55 (1.18%)
Arthritis
55 (1.18%)
Blood Glucose Increased
55 (1.18%)
Depression
55 (1.18%)
Frustration
55 (1.18%)
General Physical Health Deteriorati...
55 (1.18%)
Nervousness
55 (1.18%)
Enuresis
54 (1.16%)
Hallucination
54 (1.16%)
Hallucination, Auditory
53 (1.14%)
Hypersomnia
53 (1.14%)
Increased Appetite
53 (1.14%)
Panic Attack
53 (1.14%)
Polydipsia
53 (1.14%)
Blood Cholesterol Decreased
52 (1.12%)
Blood Glucose Decreased
52 (1.12%)
Menopause
52 (1.12%)
Mental Impairment
52 (1.12%)
Withdrawal Syndrome
52 (1.12%)
Convulsion
51 (1.1%)
Menstrual Disorder
50 (1.08%)
Tobacco User
50 (1.08%)
Anger
48 (1.03%)
Medication Error
47 (1.01%)
Fibromyalgia
42 (.9%)
Pyrexia
42 (.9%)
Amnesia
41 (.88%)
Disturbance In Attention
40 (.86%)
Feeling Abnormal
40 (.86%)
Malaise
40 (.86%)
Pain
40 (.86%)
Abdominal Pain Upper
39 (.84%)
Agitation
39 (.84%)
Alopecia
39 (.84%)
Feeling Cold
39 (.84%)
Menorrhagia
39 (.84%)
Muscle Tightness
38 (.82%)
Visual Impairment
38 (.82%)
Lice Infestation
37 (.8%)
Adverse Reaction
36 (.78%)
Dry Mouth
36 (.78%)
Dysarthria
36 (.78%)
Hormone Level Abnormal
36 (.78%)
Adverse Event
35 (.75%)
Emotional Disorder
35 (.75%)
Euphoric Mood
34 (.73%)
Parosmia
34 (.73%)
Activities Of Daily Living Impaired
32 (.69%)
Dry Throat
31 (.67%)
Bronchitis
30 (.65%)
Hypersensitivity
30 (.65%)
Chest Pain
23 (.5%)
Gait Disturbance
23 (.5%)
Paraesthesia
23 (.5%)
Glycosylated Haemoglobin Increased
22 (.47%)
Electroencephalogram Abnormal
20 (.43%)
Exercise Lack Of
19 (.41%)
Transient Ischaemic Attack
19 (.41%)
Drug Intolerance
18 (.39%)
Homicidal Ideation
18 (.39%)
Hypotension
18 (.39%)
Mental Disorder
18 (.39%)
Nicotine Dependence
18 (.39%)
Mania
17 (.37%)
Musculoskeletal Stiffness
17 (.37%)
Pain In Extremity
17 (.37%)
Road Traffic Accident
17 (.37%)
Constipation
13 (.28%)
Chronic Obstructive Pulmonary Disea...
11 (.24%)

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

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

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ExportShare/Embed Graph Export Export Data

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

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

Product Used For Unknown Indication
26
Drug Use For Unknown Indication
25
Caffeine Consumption
4
Somnolence
2
Headache
1
Ill-defined Disorder
1
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Drug Labels

LabelLabelerEffective
Coffee BeanALK-Abello, Inc.12-NOV-09
CoffeeAntigen Laboratories, Inc.12-NOV-09
CoffeeNelco Laboratories, Inc.09-DEC-09
CoffeeNelco Laboratories, Inc.09-DEC-09
CoffeeNelco Laboratories, Inc.09-DEC-09
CoffeeNelco Laboratories, Inc.09-DEC-09
Plus White Coffee Drinkers WhiteningCCA Industries, Inc.12-JUN-10
Coffee For Diagnostic Use OnlyAllergy Laboratories, Inc.11-MAR-11
Moisture Renewiced Coffee (700) Rimmel Inc.08-JUN-12
Esika Perfect Match Spf 20 Coffee SweetVentura Corporation LTD.01-FEB-13

Coffee Case Reports

What Coffee 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 Coffee. 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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