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A study for a 55-year old woman who takes Clarithromycin, Chlorpheniramine Maleate

Summary: 4 female patients aged 55 (±5) who take the same drugs are studied.

This is a personalized study for a 55 year old female patient who has Sinus infection. The study is created by eHealthMe based on reports from FDA and social media.

 

On Mar, 6, 2015: 4 females aged 52 (±5) who take Clarithromycin, Chlorpheniramine Maleate are studied

Clarithromycin, Chlorpheniramine Maleate outcomes

Information of the patient in this study:

Age: 52

Gender: female

Conditions: Sinus infection

Drugs taking:
- Clarithromycin - 500MG (clarithromycin)
- Chlorpheniramine Maleate - 12MG (chlorpheniramine maleate): used for < 1 month

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

InteractionNumber of reports on eHealthMe
Nerve Damage - Diabetic (nerve damage due to high blood sugar level)2 (50.00% of females aged 52 (±5) who take the drugs)
Hearing Loss2 (50.00% of females aged 52 (±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
Nerve Damage - Diabetic in Sinus Infection0 (0.00% of females aged 52 (±5) who have Sinus infection)
Hearing Loss in Sinus Infection2 (0.12% of females aged 52 (±5) who have Sinus infection)

(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
Nerve Damage - Diabetic in Clarithromycin2 (0.24% of females aged 52 (±5) who take Clarithromycin)
Nerve Damage - Diabetic in Chlorpheniramine Maleate0 (0.00% of females aged 52 (±5) who take Chlorpheniramine maleate)
Hearing Loss in Clarithromycin1 (0.12% of females aged 52 (±5) who take Clarithromycin)
Hearing Loss in Chlorpheniramine Maleate0 (0.00% of females aged 52 (±5) who take Chlorpheniramine maleate)

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
Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)n/an/an/an/an/an/aNerve Damage - Diabetic (nerve damage due to high blood sugar level)
Loss Of ConsciousnessHearing Loss
Hearing Loss
Toxic Epidermal Necrolysis (a rare, life-threatening skin condition that is usually caused by a reaction to drugs causes wide spread skin destruction)
Nerve Damage - Diabetic (nerve damage due to high blood sugar level)

* 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 Clarithromycin and have Nerve Damage - Diabetic
- support group for people who take Chlorpheniramine Maleate and have Nerve Damage - Diabetic
- support group for people who take Clarithromycin and have Hearing Loss
- support group for people who take Chlorpheniramine Maleate and have Hearing Loss
- support group for people who have Nerve Damage - Diabetic and Sinus infection
- support group for people who have Hearing Loss and Sinus infection
- support group for people who have Sinus Infection
- support group for people who have Hearing Loss
- support group for people who have Nerve Damage - Diabetic
- support group for people who take Chlorpheniramine Maleate
- support group for people who take Clarithromycin

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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.

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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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