Actiq and Detrol drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among 8 people who take Actiq and Detrol. Common interactions include anaemia among females, and application site pruritus among males.

The phase IV clinical study analyzes what interactions people who take Actiq and Detrol have. It is created by eHealthMe based on reports from the FDA, and is updated regularly. You may use the study as a second opinion to make health care decisions.

Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 700+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.

On Sep, 28, 2023

8 people who take Actiq and Detrol together, and have interactions are studied.

What is Actiq?

Actiq has active ingredients of fentanyl citrate. It is used in pain. Currently, eHealthMe is studying from 27,567 Actiq users.

What is Detrol?

Detrol has active ingredients of tolterodine tartrate. It is used in urge incontinence. Currently, eHealthMe is studying from 28,537 Detrol users.

Number of Actiq and Detrol reports submitted per year:

Common Actiq and Detrol drug interactions by gender *:

female:

Anaemia
Arteriosclerosis
Bladder prolapse
Bone disorder
Bone fistula
Cardiac failure congestive
Carotid artery stenosis
Cellulitis
Cerebral atrophy
Chronic inflammatory demyelinating polyradiculoneuropathy

male:

Application site pruritus
Dizziness
Gallbladder disorder
Hyperhidrosis
Insomnia
Loss of consciousness
Pyrexia
Suicidal ideation
Underweight

Common Actiq and Detrol drug interactions by age *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

n/a

40-49:

n/a

50-59:

n/a

60+:

Abscess oral
Anaemia
Chronic inflammatory demyelinating polyradiculoneuropathy
Colostomy
Contusion
Deafness
Depression
Device failure
Diarrhoea
Dysaesthesia

* Approximation only. Some reports may have incomplete information.

Do you take Actiq and Detrol?

Personalize this study to your gender and age

How to use the study?

You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.

Related studies

Drug side effects by duration, gender and age:

Actiq side effects (27,567 reports)
Detrol side effects (28,537 reports)

Common Actiq drug interactions:

Actiq and Duragesic: 24,922 reports
Actiq and Percocet: 24,575 reports
Actiq and Opana: 24,454 reports
Actiq and Opana er: 24,400 reports
Actiq and Oxycontin: 24,133 reports
Actiq and Dilaudid: 23,919 reports
Actiq and Ms contin: 23,828 reports
Actiq and Nucynta: 23,251 reports
Actiq and Hysingla er: 23,203 reports
Actiq and Butrans: 22,699 reports

Browse interactions between Actiq and drugs from A to Z:

a b c d e f g h i j k l m n o p q r s t u v w x y z

Common Detrol drug interactions:

Detrol and Detrol la: 10,882 reports
Detrol and Aspirin: 2,365 reports
Detrol and Synthroid: 2,004 reports
Detrol and Lipitor: 1,997 reports
Detrol and Nexium: 1,647 reports
Detrol and Prednisone: 1,478 reports
Detrol and Lisinopril: 1,474 reports
Detrol and Baclofen: 1,430 reports
Detrol and Celebrex: 1,337 reports
Detrol and Lasix: 1,325 reports

Browse interactions between Detrol and drugs from A to Z:

a b c d e f g h i j k l m n o p q r s t u v w x y z

How the study uses the data?

The study uses data from the FDA. It is based on fentanyl citrate and tolterodine tartrate (the active ingredients of Actiq and Detrol, respectively), and Actiq and Detrol (the brand names). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study. Patients in the study may take other drugs besides Actiq and Detrol.

Who is eHealthMe?

With medical big data and proven AI algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 700+ medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).

WARNING, DISCLAIMER, USE FOR PUBLICATION

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only. Our phase IV clinical studies alone cannot establish cause-effect relationship. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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