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TILIDINE

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Tilidine Adverse Events Reported to the FDA Over Time

How are Tilidine adverse event reports trending over time?

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

Most Common Tilidine Adverse Events Reported to the FDA

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

Suicide Attempt
19 (3.39%)
Somnolence
18 (3.21%)
Drug Interaction
16 (2.86%)
Intentional Overdose
12 (2.14%)
Apathy
11 (1.96%)
Convulsion
11 (1.96%)
Loss Of Consciousness
11 (1.96%)
Paralysis
11 (1.96%)
Confusional State
10 (1.79%)
Nausea
10 (1.79%)
Haematemesis
9 (1.61%)
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Tachycardia
9 (1.61%)
Aphasia
8 (1.43%)
Dizziness
8 (1.43%)
Flushing
8 (1.43%)
Headache
8 (1.43%)
Pupillary Reflex Impaired
8 (1.43%)
Disorientation
7 (1.25%)
Hallucination, Visual
7 (1.25%)
Hypoaesthesia
7 (1.25%)
Multiple Drug Overdose Intentional
7 (1.25%)
Muscle Rigidity
7 (1.25%)
Pneumonia
7 (1.25%)
Withdrawal Syndrome
7 (1.25%)
Blindness Transient
6 (1.07%)
Drug Toxicity
6 (1.07%)
Abdominal Pain
5 (.89%)
Amnesia
5 (.89%)
Coma
5 (.89%)
Dyspnoea
5 (.89%)
Speech Disorder
5 (.89%)
Trance
5 (.89%)
Vomiting
5 (.89%)
Gait Disturbance
4 (.71%)
Haemoptysis
4 (.71%)
Hypertension
4 (.71%)
Insomnia
4 (.71%)
Memory Impairment
4 (.71%)
Muscle Spasticity
4 (.71%)
Overdose
4 (.71%)
Pain
4 (.71%)
Painful Respiration
4 (.71%)
Paraesthesia
4 (.71%)
Tongue Biting
4 (.71%)
Tremor
4 (.71%)
Unresponsive To Stimuli
4 (.71%)
Blindness
3 (.54%)
Blood Gases Abnormal
3 (.54%)
Blood Pressure Increased
3 (.54%)
Bradycardia
3 (.54%)
C-reactive Protein Increased
3 (.54%)
Cognitive Disorder
3 (.54%)
Completed Suicide
3 (.54%)
Congenital Choroid Plexus Cyst
3 (.54%)
Convulsion Neonatal
3 (.54%)
Csf Protein Increased
3 (.54%)
Cyst
3 (.54%)
Delirium
3 (.54%)
Depression
3 (.54%)
Drooling
3 (.54%)
Drug Intolerance
3 (.54%)
Foot Fracture
3 (.54%)
Hyponatraemia
3 (.54%)
Lethargy
3 (.54%)
Restless Legs Syndrome
3 (.54%)
Self Injurious Behaviour
3 (.54%)
Stupor
3 (.54%)
Weight Increased
3 (.54%)
Abdominal Pain Upper
2 (.36%)
Acute Prerenal Failure
2 (.36%)
Agitation
2 (.36%)
Agranulocytosis
2 (.36%)
Alanine Aminotransferase Increased
2 (.36%)
Alkalosis
2 (.36%)
Blood Cholesterol Increased
2 (.36%)
Blood Creatinine Increased
2 (.36%)
Blood Urea Increased
2 (.36%)
Cardiac Disorder
2 (.36%)
Chest Pain
2 (.36%)
Chills
2 (.36%)
Constipation
2 (.36%)
Cystitis
2 (.36%)
Dehydration
2 (.36%)
Drug Ineffective
2 (.36%)
Dry Skin
2 (.36%)
Fall
2 (.36%)
Fatigue
2 (.36%)
General Physical Health Deteriorati...
2 (.36%)
Hepatic Enzyme Increased
2 (.36%)
Herpes Zoster
2 (.36%)
Hypokalaemia
2 (.36%)
Hypotension
2 (.36%)
Liver Disorder
2 (.36%)
Malaise
2 (.36%)
Meningitis
2 (.36%)
Neuralgia
2 (.36%)
Neurogenic Bladder
2 (.36%)
Nightmare
2 (.36%)
Normochromic Normocytic Anaemia
2 (.36%)
Nystagmus
2 (.36%)
Odynophagia
2 (.36%)

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

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

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

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

Pain
44
Drug Use For Unknown Indication
33
Product Used For Unknown Indication
17
Rheumatoid Arthritis
15
Arthralgia
11
Neuralgia
11
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Back Pain
5
Suicide Attempt
5
Ankylosing Spondylitis
4
Major Depression
3
Diabetic Neuropathy
3
Trigeminal Neuralgia
3
Proctalgia
2
Osteoporosis
2
Complex Regional Pain Syndrome
2
Polyarthritis
2
Bone Pain
2
Restless Legs Syndrome
2
Intentional Drug Misuse
2
Arthritis
2
Neck Pain
2
Analgesic Therapy
2
Polyneuropathy
1
Dependence
1
Analgesia
1
Depression
1
Migraine
1
Fibromyalgia
1
Cancer Pain
1
Opiates
1
Musculoskeletal Pain
1

Tilidine Case Reports

What Tilidine 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 Tilidine. 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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