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SEPTOCAINE

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Septocaine Adverse Events Reported to the FDA Over Time

How are Septocaine adverse event reports trending over time?

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

Most Common Septocaine Adverse Events Reported to the FDA

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

Hypoaesthesia Oral
60 (6.05%)
Paraesthesia
56 (5.65%)
Hypoaesthesia
46 (4.64%)
Paraesthesia Oral
37 (3.73%)
Anaesthetic Complication
22 (2.22%)
Dysgeusia
22 (2.22%)
Nerve Injury
21 (2.12%)
Dizziness
18 (1.82%)
Pain
18 (1.82%)
Ageusia
16 (1.61%)
Swelling Face
16 (1.61%)
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Burning Sensation
15 (1.51%)
Glossodynia
15 (1.51%)
Post Procedural Complication
14 (1.41%)
Nausea
13 (1.31%)
Anxiety
12 (1.21%)
Speech Disorder
12 (1.21%)
Tremor
10 (1.01%)
Dysphagia
9 (.91%)
Injection Site Pain
8 (.81%)
Loss Of Consciousness
8 (.81%)
Swelling
8 (.81%)
Dyspnoea
7 (.71%)
Fatigue
7 (.71%)
Blood Pressure Increased
6 (.61%)
Chest Pain
6 (.61%)
Convulsion
6 (.61%)
Dry Mouth
6 (.61%)
Headache
6 (.61%)
Hypogeusia
6 (.61%)
Lip Swelling
6 (.61%)
Swollen Tongue
6 (.61%)
Tongue Disorder
6 (.61%)
Trismus
6 (.61%)
Disorientation
5 (.5%)
Dysaesthesia
5 (.5%)
Facial Pain
5 (.5%)
Gingival Disorder
5 (.5%)
Heart Rate Increased
5 (.5%)
Hypoaesthesia Facial
5 (.5%)
Jaw Disorder
5 (.5%)
Muscle Tightness
5 (.5%)
Pallor
5 (.5%)
Palpitations
5 (.5%)
Urticaria
5 (.5%)
Amnesia
4 (.4%)
Angioedema
4 (.4%)
Asthenia
4 (.4%)
Confusional State
4 (.4%)
Erythema
4 (.4%)
Heart Rate Decreased
4 (.4%)
Hypertension
4 (.4%)
Incorrect Route Of Drug Administrat...
4 (.4%)
Malaise
4 (.4%)
Memory Impairment
4 (.4%)
Muscle Contractions Involuntary
4 (.4%)
Nervousness
4 (.4%)
Pain In Jaw
4 (.4%)
Restlessness
4 (.4%)
Syncope
4 (.4%)
Anaphylactic Reaction
3 (.3%)
Anosmia
3 (.3%)
Blister
3 (.3%)
Bone Disorder
3 (.3%)
Bronchospasm
3 (.3%)
Chills
3 (.3%)
Cold Sweat
3 (.3%)
Contraindication To Medical Treatme...
3 (.3%)
Contusion
3 (.3%)
Delayed Recovery From Anaesthesia
3 (.3%)
Discomfort
3 (.3%)
Drug Effect Prolonged
3 (.3%)
Drug Hypersensitivity
3 (.3%)
Drug Ineffective
3 (.3%)
Drug Interaction
3 (.3%)
Exophthalmos
3 (.3%)
Fear
3 (.3%)
Feeling Abnormal
3 (.3%)
Feeling Hot
3 (.3%)
Gingival Pain
3 (.3%)
Hypersensitivity
3 (.3%)
Iatrogenic Injury
3 (.3%)
Medication Error
3 (.3%)
Myalgia
3 (.3%)
Oedema Mouth
3 (.3%)
Oral Discomfort
3 (.3%)
Oral Pain
3 (.3%)
Retinal Vein Occlusion
3 (.3%)
Thinking Abnormal
3 (.3%)
Tooth Disorder
3 (.3%)
Vision Blurred
3 (.3%)
Vocal Cord Paralysis
3 (.3%)
Vomiting
3 (.3%)
Abdominal Discomfort
2 (.2%)
Alopecia
2 (.2%)
Arrhythmia
2 (.2%)
Blindness
2 (.2%)
Blindness Unilateral
2 (.2%)
Blood Pressure Decreased
2 (.2%)
Chest Discomfort
2 (.2%)
Diarrhoea
2 (.2%)

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

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

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

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

Local Anaesthesia
177
Anaesthesia
15
Dental Operation
11
Tooth Extraction
10
Endodontic Procedure
10
Tooth Repair
9
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Tooth Disorder
8
Dental Care
7
Dental Treatment
7
Nerve Block
5
Dental Caries
5
Artificial Crown Procedure
4
Injury
2
Hypoaesthesia
2
Jaw Disorder
1
Tooth Abscess
1
Hypoaesthesia Oral
1
Premedication
1
Disability
1
Dental Prosthesis Placement
1
Drug Use For Unknown Indication
1
Skin Test
1
Anaesthesia Procedure
1
Dental Cleaning
1
Analgesic Therapy
1
Gingival Disorder
1
Dental Disorder Prophylaxis
1
Analgesic Effect
1
Pain Management
1
Infiltration Anaesthesia
1
Periodontitis
1
Dental Cosmetic Procedure
1
Hypersensitivity
1
Surgery
1
Wisdom Teeth Removal
1

Drug Labels

LabelLabelerEffective
Septocaine And EpinephrineSeptodont Inc.01-FEB-11

Septocaine Case Reports

What Septocaine 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 Septocaine. 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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