Cognex and Pepcid drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Cognex (tacrine hydrochloride) and Pepcid (famotidine). Common drug interactions include appetite decreased among females and abdominal pain among males.
The phase IV clinical study analyzes what interactions people have when they take Cognex and Pepcid. It is created by eHealthMe based on reports of 15 people who take the same drugs from the FDA, and is updated regularly.
What is Cognex?
Cognex has active ingredients of tacrine hydrochloride. eHealthMe is studying from 740 Cognex users. Check the latest studies of Cognex.
What is Pepcid?
Pepcid has active ingredients of famotidine. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 55,774 Pepcid users. Check the latest studies of Pepcid.
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 >>>.
15 people who take Cognex and Pepcid together, and have interactions are studied.

What are the common drug interactions of Cognex and Pepcid, by gender? *:
female:
- Appetite decreased (decreased appetite occurs when you have a reduced desire to eat)
- Nausea (feeling of having an urge to vomit)
- Vomiting
- Apathy
- Depression
- Headache (pain in head)
- Irritability
- Abdominal pain
- Aggression
- Agitation (state of anxiety or nervous excitement)
male:
- Abdominal pain
- Agitation (state of anxiety or nervous excitement)
- Blood cholesterol increased
- Depression
- Diarrhoea
- Disinhibition (loss of inhibition)
- Hallucination (an experience involving the perception of something not present)
- Insomnia (sleeplessness)
- Irritability
- Low density lipoprotein increased (cholesterol increased in blood)
What are the common drug interactions of Cognex and Pepcid, 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:
n/a
50-59:
n/a
60+:
- Nausea (feeling of having an urge to vomit)
- Vomiting
- Hallucination (an experience involving the perception of something not present)
- Headache (pain in head)
- Insomnia (sleeplessness)
- Weight decreased
- Abdominal pain upper
- Aggression
- Akinesia (loss of control of voluntary muscle movements)
- Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
* Approximation only. Some reports may have incomplete information.
Do you take Cognex and Pepcid?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Cognex and Pepcid:
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 Cognex:
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 Pepcid:
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 Cognex 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 Pepcid 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 tacrine hydrochloride and famotidine (the active ingredients of Cognex and Pepcid, respectively), and Cognex and Pepcid (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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