Ranitidine hydrochloride and Adcetris drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported only by a few people who take Ranitidine hydrochloride and Adcetris together.
The phase IV clinical study analyzes what interactions people who take Ranitidine hydrochloride and Adcetris have. It is created by eHealthMe based on reports of 3 people who take the same drugs from the FDA, and is updated regularly.
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 600+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.
3 people who take Ranitidine hydrochloride and Adcetris together, and have interactions are studied.
What is Ranitidine hydrochloride?
Ranitidine hydrochloride has active ingredients of ranitidine hydrochloride. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 67,576 Ranitidine hydrochloride users for its effectiveness, alternative drugs and more.
What is Adcetris?
Adcetris has active ingredients of brentuximab vedotin. eHealthMe is studying from 4,136 Adcetris users for its effectiveness, alternative drugs and more.
Number of Ranitidine hydrochloride and Adcetris reports submitted per year:

Common Ranitidine Hydrochloride and Adcetris drug interactions by gender *:
female:
n/a
male:
- Blood lactate dehydrogenase increased
- Blood sodium decreased
- Pathogen resistance
- Renal failure acute
- Sepsis
- Cytokine release syndrome
- Dehydration
- Diabetic hyperosmolar coma
- Hyperglycaemia
- Hypotension
Common Ranitidine Hydrochloride and Adcetris 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:
- Pathogen resistance
- Renal failure acute
- Sepsis
- Blood sodium decreased
- Dehydration
- Diabetic hyperosmolar coma
- Hyperglycaemia
- Oedema
60+:
- Blood lactate dehydrogenase increased
- Cytokine release syndrome
- Hypotension
- Lactic acidosis
- Oliguria
* Approximation only. Some reports may have incomplete information.
Do you take Ranitidine hydrochloride and Adcetris?
Personalize this study to your gender and ageHow 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
Alternative drugs to, pros and cons of the 2 drugs:
- Ranitidine hydrochloride (67,576 reports)
- Adcetris (4,136 reports)
Browse all drug interactions of Ranitidine hydrochloride and Adcetris:
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 zCommon Ranitidine hydrochloride side effects:
- Breast cancer: 9,833 reports
- Prostate cancer: 9,229 reports
- Colon cancer: 7,581 reports
- Renal cell carcinoma (a kidney cancer): 7,071 reports
- Bladder cancer: 5,798 reports
- Gastric cancer (stomach cancer): 2,606 reports
- Pancreatic carcinoma (pancreatic cancer): 2,582 reports
- Chronic kidney disease: 1,307 reports
- Thyroid cancer: 1,027 reports
Browse all side effects of Ranitidine hydrochloride:
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 zCommon Adcetris side effects:
- Fever: 270 reports
- Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection): 245 reports
- Death: 229 reports
- Hodgkin's lymphoma (cancer originating from white blood cells): 215 reports
- Thrombocytopenia (decrease of platelets in blood): 182 reports
- Rashes (redness): 180 reports
- Pneumonia: 169 reports
Browse all side effects of Adcetris:
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 zCommon Ranitidine hydrochloride interactions:
- Ranitidine hydrochloride and Ranitidine: 18,826 reports
- Ranitidine hydrochloride and Omeprazole: 1,523 reports
- Ranitidine hydrochloride and Pantoprazole: 1,332 reports
- Ranitidine hydrochloride and Nexium: 1,323 reports
- Ranitidine hydrochloride and Protonix: 1,172 reports
- Ranitidine hydrochloride and Prilosec: 1,159 reports
- Ranitidine hydrochloride and Prevacid: 1,145 reports
- Ranitidine hydrochloride and Aspirin: 1,142 reports
- Ranitidine hydrochloride and Furosemide: 1,066 reports
- Ranitidine hydrochloride and Lisinopril: 911 reports
Browse all interactions between Ranitidine hydrochloride 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 zCommon Adcetris interactions:
- Adcetris and Dacarbazine: 640 reports
- Adcetris and Cyclophosphamide: 323 reports
- Adcetris and Prednisone: 232 reports
- Adcetris and Vinblastine sulfate: 222 reports
- Adcetris and Etoposide: 206 reports
- Adcetris and Prednisolone: 175 reports
- Adcetris and Carboplatin: 106 reports
- Adcetris and Paracetamol: 101 reports
Browse all interactions between Adcetris 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 ranitidine hydrochloride and brentuximab vedotin (the active ingredients of Ranitidine hydrochloride and Adcetris, respectively), and Ranitidine hydrochloride and Adcetris (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 Ranitidine hydrochloride and Adcetris.
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 600+ 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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