Tegsedi and Pantoprazole sodium drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Tegsedi (inotersen sodium) and Pantoprazole sodium (pantoprazole sodium). Common drug interactions include urinary occult blood positive among females and white blood cell count decreased among males.
The phase IV clinical study analyzes what interactions people have when they take Tegsedi and Pantoprazole sodium. It is created by eHealthMe based on reports of 40 people who take the same drugs from the FDA, and is updated regularly.
What is Tegsedi?
Tegsedi has active ingredients of inotersen sodium. eHealthMe is studying from 2,040 Tegsedi users. Check the latest studies of Tegsedi.
What is Pantoprazole sodium?
Pantoprazole sodium has active ingredients of pantoprazole sodium. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 66,892 Pantoprazole sodium users. Check the latest studies of Pantoprazole sodium.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
40 people who take Tegsedi and Pantoprazole sodium together, and have interactions are studied.

What are the common drug interactions of Tegsedi and Pantoprazole Sodium, by gender? *:
female:
- Urinary occult blood positive
- Nausea (feeling of having an urge to vomit)
- Arthralgia (joint pain)
- Urine leukocyte esterase positive
- White blood cells urine positive
- Adverse drug reaction
- Ageusia (loss of taste functions of the tongue)
- Dizziness postural
- Fatigue (feeling of tiredness)
- Headache (pain in head)
male:
- White blood cell count decreased
- Diarrhoea
- Blood albumin decreased
- Blood lactate dehydrogenase increased
- Blood magnesium decreased
- Fatigue (feeling of tiredness)
- Malaise (a feeling of general discomfort or uneasiness)
- Mean cell haemoglobin decreased (less than normal haemoglobin per red blood cell in a sample of blood)
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Red cell distribution width increased
What are the common drug interactions of Tegsedi and Pantoprazole Sodium, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Adverse drug reaction
- Fatigue (feeling of tiredness)
- Headache (pain in head)
- Influenza like illness
- Injection site erythema (redness at injection site)
- Nausea (feeling of having an urge to vomit)
- Pain
- Protein urine present
- Visual impairment
- Bacterial test positive
50-59:
- Haematocrit decreased
- Haemoglobin decreased
- High density lipoprotein decreased
- Lymphocyte count decreased
- Malaise (a feeling of general discomfort or uneasiness)
- Platelet count decreased
- Platelet disorder
- Protein urine present
- Red blood cell burr cells present
- Red blood cell count decreased
60+:
- Platelet count decreased
- Glomerular filtration rate decreased
- Fungal test positive
- Protein urine present
- Renal failure (kidney dysfunction)
- Renal impairment (severely reduced kidney function)
- Urinary occult blood positive
- Diarrhoea
- Arthralgia (joint pain)
- Aspartate aminotransferase increased
What are the existing conditions these people have? *
- Hereditary Neuropathic Amyloidosis (hereditary- diseases resulting from abnormal deposition of certain proteins (amyloid) in various bodily areas by problems with signals from the nerves): 36 people, 90.00%
- Peripheral Arterial Occlusive Disease (reproducible ischemic muscle pain): 3 people, 7.50%
- High Blood Pressure: 3 people, 7.50%
- Gout (uric acid crystals building up in the body): 3 people, 7.50%
- Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures): 3 people, 7.50%
- Enlarged Prostate: 3 people, 7.50%
- Type 2 Diabetes: 2 people, 5.00%
- Peripheral Vascular Disorder: 2 people, 5.00%
- Oedema (fluid collection in tissue): 2 people, 5.00%
- Neuralgia (pain in one or more nerves): 2 people, 5.00%
* Approximation only. Some reports may have incomplete information.
Do you take Tegsedi and Pantoprazole sodium?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Tegsedi (2,040 reports)
- Pantoprazole sodium (66,892 reports)
Browse all drug interactions of Tegsedi and Pantoprazole sodium:
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 zSub-studies by gender and age:
Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Tegsedi:
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 zBrowse all side effects of Pantoprazole sodium:
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 zBrowse all interactions between Tegsedi 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 zBrowse all interactions between Pantoprazole sodium 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 zHow the study uses the data?
The study uses data from the FDA. It is based on inotersen sodium and pantoprazole sodium (the active ingredients of Tegsedi and Pantoprazole sodium, respectively), and Tegsedi and Pantoprazole sodium (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.
How to use the study?
DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.
Who is eHealthMe?
With medical big data and proven AI/ML 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 800+ peer-reviewed 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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