Zantac and Parlodel drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Zantac (ranitidine hydrochloride) and Parlodel (bromocriptine mesylate). Common drug interactions include dysuria among females and depressed level of consciousness among males.
The phase IV clinical study analyzes what interactions people have when they take Zantac and Parlodel. It is created by eHealthMe based on reports of 20 people who take the same drugs from the FDA, and is updated regularly.
What is Zantac?
Zantac has active ingredients of ranitidine hydrochloride. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 434,161 Zantac users. Check the latest studies of Zantac.
What is Parlodel?
Parlodel has active ingredients of bromocriptine mesylate. eHealthMe is studying from 2,327 Parlodel users. Check the latest studies of Parlodel.
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 >>>.
20 people who take Zantac and Parlodel together, and have interactions are studied.

What are the common drug interactions of Zantac and Parlodel, by gender? *:
female:
- Dysuria (painful or difficult urination)
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Contusion (a type of hematoma of tissue in which capillaries)
- Crying
- Depression
- Disturbance in attention
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Heart rate increased
male:
- Depressed level of consciousness
- Speech disorder
- Drug toxicity
- Ileus (a painful obstruction of the ileum or other part of the intestine)
- Incontinence (lack of moderation or self-control)
- Nausea (feeling of having an urge to vomit)
- Oral mucosal discolouration (change in colour of mucous membrane of mouth)
- Anorexia (eating disorder characterized by immoderate food restriction and irrational fear of gaining weight)
- C-reactive protein increased
- Cardiac failure
What are the common drug interactions of Zantac and Parlodel, 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:
- Colitis (inflammation of colon)
- Hypotension (abnormally low blood pressure)
- Vasospasm (sudden constriction of a blood vessel, reducing its diameter and flow rate)
- Visual field defect
50-59:
- Dysuria (painful or difficult urination)
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Contusion (a type of hematoma of tissue in which capillaries)
- Crying
- Depression
- Disturbance in attention
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Heart rate increased
60+:
- Depressed level of consciousness
- Speech disorder
- Drug toxicity
- Ileus (a painful obstruction of the ileum or other part of the intestine)
- Incontinence (lack of moderation or self-control)
- Nausea (feeling of having an urge to vomit)
- Oral mucosal discolouration (change in colour of mucous membrane of mouth)
- Rash erythematous (redness of the skin)
- Anorexia (eating disorder characterized by immoderate food restriction and irrational fear of gaining weight)
- Application site erythema (redness of the skin at application site)
What are the existing conditions these people have? *
- Insomnia (sleeplessness): 6 people, 30.00%
- Herpes Zoster: 4 people, 20.00%
- Depression: 3 people, 15.00%
- High Blood Cholesterol: 3 people, 15.00%
- Stress And Anxiety: 2 people, 10.00%
- Constipation: 2 people, 10.00%
- Gastritis (inflammation of stomach): 2 people, 10.00%
- Glaucoma (increased fluid pressure in the eye with vision loss): 2 people, 10.00%
- High Blood Pressure: 2 people, 10.00%
- Hypertriglyceridaemia (excess of triglycerides in the blood): 2 people, 10.00%
* Approximation only. Some reports may have incomplete information.
Do you take Zantac and Parlodel?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Zantac and Parlodel:
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 Zantac:
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 Parlodel:
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 Zantac 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 Parlodel 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 bromocriptine mesylate (the active ingredients of Zantac and Parlodel, respectively), and Zantac and Parlodel (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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