Who have Hyperacusis with Carbidopa - from FDA reports
There is no Hyperacusis reported by people who take Carbidopa yet. This review analyzes which people have Hyperacusis with Carbidopa. It is created by eHealthMe based on reports from FDA, and is updated regularly.
How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.
Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our original studies have been referenced on 500+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO. On eHealthMe, you can research drugs and monitor them (see testimonials). If you find eHealthMe useful, please help us to spread the words below or leave us a testimonial.
No report is found.
Do you have Hyperacusis while taking Carbidopa?
- Check whether a drug or a condition causes Hyperacusis
- Subscribe to monitor Hyperacusis in Carbidopa
You are not alone:
Carbidopa has active ingredients of carbidopa. It is often used in parkinson's disease. (latest outcomes from Carbidopa 1,069 users)
Hyperacusis (disorder in loudness perception) has been reported by people with depression, stress and anxiety, pain, migraine, multiple sclerosis (latest reports from 2,755 Hyperacusis patients).
Drugs that are associated with HyperacusisHyperacusis
Could your condition cause HyperacusisHyperacusis
Carbidopa side effects
- Carbidopa side effects (969 reports)
Browse by gender and age
Browse all side effects of Carbidopaa b c d e f g h i j k l m n o p q r s t u v w x y z
What would happen?
Recent general studies
- Will you have Candidiasis with Fungizone? - now
- Will you have Drowsiness with Abstral? - 2 seconds ago
- Ampyra and Halada drug interaction - 2 seconds ago
- Will you have Somnolence with Abstral? - 2 seconds ago
- Will you have Sleepy with Abstral? - 3 seconds ago
- Will you have Sleepiness with Abstral? - 3 seconds ago
- Will you have Hypersomnia with Abstral? - 3 seconds ago
- Will you have Drowsiness, Hypersomnia, Sleepiness - During The Day, Somnolence with Abstral? - 4 seconds ago
- Will you have Can'T Stay Wake with Abstral? - 4 seconds ago
- Will you have Can'T Stay Awake with Abstral? - 4 seconds ago
Recent personal studies
- A study for a 65 year old woman who takes Enbrel - 2 hours ago
- A study for a 82 year old man who takes Lyrica - 4 hours ago
- A study for a 64 year old man who takes Amlodipine Besylate; Benazepril Hydrochloride - 4 hours ago
- A study for a 62 year old woman who takes Losartan Potassium - 4 hours ago
- A study for a 88 year old man who takes Tylenol, Azithromycin - 5 hours ago
- Prediction of Levonorgestrel;ethinyl;estradiol;ethinyl;estradiol for a 26 year old woman - 6 hours ago
- Prediction of Desogestrel; Ethinylestradiol; Ethinyl Estradiol for a 26 year old woman - 6 hours ago
- Prediction of Crestor for a 70 year old man - 6 hours ago
- A study for a 40 year old woman who takes Zoloft, Vivitrol - 7 hours ago
- A study for a 71 year old woman who takes Losartan Potassium, Levothyroxine Sodium, Lantus Solostar, Glimepiride, Tramadol - 7 hours ago
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT 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.