DrugCite
Search

SCOPOLAMINE

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Scopolamine Adverse Events Reported to the FDA Over Time

How are Scopolamine adverse event reports trending over time?

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

Most Common Scopolamine Adverse Events Reported to the FDA

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

Off Label Use
61 (3.19%)
Nausea
45 (2.35%)
Agitation
39 (2.04%)
Hallucination
36 (1.88%)
Overdose
34 (1.78%)
Confusional State
33 (1.73%)
Dry Mouth
32 (1.67%)
Dizziness
30 (1.57%)
Vomiting
29 (1.52%)
Fall
27 (1.41%)
Headache
21 (1.1%)
Show More Show More
Tachycardia
20 (1.05%)
Wrong Technique In Drug Usage Proce...
20 (1.05%)
Disorientation
19 (.99%)
Pain
19 (.99%)
Anticholinergic Syndrome
18 (.94%)
Mydriasis
17 (.89%)
Somnolence
17 (.89%)
Delirium
16 (.84%)
Malaise
16 (.84%)
Neutrophil Count Increased
16 (.84%)
White Blood Cell Count Increased
16 (.84%)
Constipation
15 (.78%)
Loss Of Consciousness
15 (.78%)
Completed Suicide
14 (.73%)
Mechanical Ventilation
14 (.73%)
Weight Decreased
14 (.73%)
Anxiety
13 (.68%)
Neutropenia
13 (.68%)
White Blood Cell Count Decreased
13 (.68%)
Fatigue
12 (.63%)
Tremor
12 (.63%)
Visual Impairment
12 (.63%)
Abdominal Pain
11 (.58%)
Diarrhoea
11 (.58%)
Productive Cough
11 (.58%)
Vision Blurred
11 (.58%)
Balance Disorder
10 (.52%)
Drug Interaction
10 (.52%)
Dyskinesia
10 (.52%)
Mental Status Changes
10 (.52%)
Muscle Spasms
10 (.52%)
Seasonal Allergy
10 (.52%)
Unresponsive To Stimuli
10 (.52%)
Platelet Count Decreased
9 (.47%)
Rash
9 (.47%)
Anaemia
8 (.42%)
Blood Alkaline Phosphatase Increase...
8 (.42%)
Coordination Abnormal
8 (.42%)
Diplopia
8 (.42%)
Dysarthria
8 (.42%)
Dyspnoea
8 (.42%)
Hallucination, Auditory
8 (.42%)
Inappropriate Schedule Of Drug Admi...
8 (.42%)
Persecutory Delusion
8 (.42%)
Pruritus
8 (.42%)
Restlessness
8 (.42%)
Salivary Hypersecretion
8 (.42%)
Abnormal Behaviour
7 (.37%)
Anger
7 (.37%)
Asthenia
7 (.37%)
Atrial Fibrillation
7 (.37%)
Convulsion
7 (.37%)
Death
7 (.37%)
Drug Hypersensitivity
7 (.37%)
Drug Ineffective
7 (.37%)
Drug Ineffective For Unapproved Ind...
7 (.37%)
Febrile Neutropenia
7 (.37%)
Multiple Drug Overdose
7 (.37%)
Pneumonia Fungal
7 (.37%)
Psychotic Disorder
7 (.37%)
Sedation
7 (.37%)
Thermal Burn
7 (.37%)
Thrombocytopenia
7 (.37%)
Vertigo
7 (.37%)
Alanine Aminotransferase Increased
6 (.31%)
Application Site Irritation
6 (.31%)
Clostridium Difficile Colitis
6 (.31%)
Cough
6 (.31%)
Dry Eye
6 (.31%)
Dysphagia
6 (.31%)
Hallucination, Visual
6 (.31%)
Ideas Of Reference
6 (.31%)
Liver Function Test Abnormal
6 (.31%)
Mental Disorder
6 (.31%)
Microcytic Anaemia
6 (.31%)
Post Procedural Complication
6 (.31%)
Red Blood Cell Elliptocytes Present
6 (.31%)
Transient Ischaemic Attack
6 (.31%)
Wound Secretion
6 (.31%)
Abasia
5 (.26%)
Application Site Pain
5 (.26%)
Blood Pressure Increased
5 (.26%)
Concomitant Disease Progression
5 (.26%)
Dehydration
5 (.26%)
Depressed Level Of Consciousness
5 (.26%)
Drug Toxicity
5 (.26%)
Faecaloma
5 (.26%)
Feeling Abnormal
5 (.26%)
Flushing
5 (.26%)
Fungal Rhinitis
5 (.26%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Product Used For Unknown Indication
108
Abdominal Pain
65
Nausea
55
Salivary Hypersecretion
46
Irritable Bowel Syndrome
46
Motion Sickness
44
Show More Show More
Drug Use For Unknown Indication
40
Pain
27
Abdominal Pain Upper
21
Prophylaxis Of Nausea And Vomiting
20
Vomiting
19
Premedication
17
Gastric Ulcer
15
Prophylaxis
13
Prophylaxis Against Motion Sickness
12
Crohns Disease
12
Gastritis
10
Abdominal Discomfort
9
Diarrhoea
9
Gastric Disorder
9
Palliative Care
8
Gastrooesophageal Reflux Disease
7
Dizziness
7
Anxiety
6
Muscle Spasms
6
Back Pain
5
Increased Bronchial Secretion
5
Drooling
5
Malaise
5
Bronchial Obstruction
4
Dysmenorrhoea
4
Gastrointestinal Disorder
4
Pain Management
3
Anaesthesia
3
Intestinal Spasm
3
Gastrointestinal Obstruction
3
General Anaesthesia
3
Vertigo
3
Flatulence
3
Analgesic Therapy
3
Procedural Nausea
3
Gastrointestinal Hypomotility
3
Diverticulitis
2
Supportive Care
2
Convulsion
2
Gastrointestinal Disorder Therapy
2
Endoscopy Upper Gastrointestinal Tr...
2
Cholelithiasis
2
Gastrointestinal Pain
2
Sleep Disorder
2
Smoking Cessation Therapy
2

Drug Labels

LabelLabelerEffective
Isopto Hyoscine Alcon Laboratories, Inc.01-JUN-07
Scopolamine HydrobromideAPP Pharmaceuticals, LLC30-AUG-12

Scopolamine Case Reports

What Scopolamine safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Scopolamine. 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.

Comments

Share your experience with Scopolamine.