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A study for a 32-year old man who takes Famotidine, Carisoprodol, Tylenol W/ Codeine No. 3

Summary: 21 male patients aged 32 (±5) who take the same drugs are studied.

This is a personalized study for a 32 year old male patient who has GERD. The study is created by eHealthMe based on reports from FDA and social media.

 

On Mar, 3, 2015: 21 males aged 29 (±5) who take Famotidine, Carisoprodol, Tylenol W/ Codeine No. 3 are studied

Famotidine, Carisoprodol, Tylenol W/ Codeine No. 3 outcomes

Information of the patient in this study:

Age: 29

Gender: male

Conditions: GERD, Whiplash Injury

Drugs taking:
- Famotidine - 20MG (famotidine): used for < 1 month
- Carisoprodol - 350MG (carisoprodol): used for < 1 month
- Tylenol W/ Codeine No. 3 - 300MG;30MG (acetaminophen; codeine phosphate): used for < 1 month

Drug interactions have: most severe constipation aggravated

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

InteractionNumber of reports on eHealthMe
Constipation Aggravated (worse constipation)0 (0.00% of males aged 29 (±5) who take the drugs)

(as an adverse outcome could be a symptom of a condition, additional studies are listed to help identify the cause: for example, regardless of which drug is taken, how many female HBP patients aged 50 (±5) have nausea)

Symptom (click a symptom for in-depth analysis)Number of reports on eHealthMe
Constipation Aggravated in Gerd7 (1.30% of males aged 29 (±5) who have Gerd)
Constipation Aggravated in Whiplash Injury1 (25.00% of males aged 29 (±5) who have Whiplash injury)

(as an adverse outcome could be a side effect of a drug, additional studies are listed to help identify the cause: for example, how many female Aspirin users aged 50 (±5) have nausea)

Side effect (click a side effect for in-depth analysis)Number of reports on eHealthMe
Constipation Aggravated in Famotidine6 (1.56% of males aged 29 (±5) who take Famotidine)
Constipation Aggravated in Carisoprodol1 (1.47% of males aged 29 (±5) who take Carisoprodol)
Constipation Aggravated in Tylenol W/ Codeine No. 31 (0.94% of males aged 29 (±5) who take Tylenol w/ codeine no. 3)

Drug effectiveness over time :

n/a

Most common drug interactions over time * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ yearsnot specified
n/an/an/an/an/an/an/aGait Disturbance
Arthralgia (joint pain)
Muscular Weakness (muscle weakness)
Musculoskeletal Discomfort (discomfort in the body's muscles, joints, tendons, ligaments and nerves)
Hypoaesthesia (reduced sense of touch or sensation)
Erythema (redness of the skin)
Oedema Peripheral (superficial swelling)
Emphysema (chronic respiratory disease - over inflation of the air sacs (alveoli) in the lungs)
Impaired Healing
Dry Mouth

* Some reports may have incomplete information.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

You can also:

 

 

 

You are not alone! Join a related mobile support group on :
- support group for people who take Famotidine and have Constipation Aggravated
- support group for people who take Carisoprodol and have Constipation Aggravated
- support group for people who take Tylenol W/ Codeine No. 3 and have Constipation Aggravated
- support group for people who have GERD
- support group for people who have Constipation Aggravated
- support group for people who take Carisoprodol
- support group for people who take Famotidine
- support group for people who take Tylenol W/ Codeine No. 3

Recent related drug studies (Check your drugs):

Related drug interaction studies:

Drug effectiveness in real world:

In-depth study of side effects (who have it, when it happens and how):

Complete drug side effects:

Alternative drugs:

Drugs associated with:

Conditions associated with:

NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

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, and has not been supported by scientific studies or clinical trials unless otherwise stated. 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.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

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

   

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