Dantrium and Slow rhr - from FDA reports
Slow rhr is found among people who take Dantrium, especially for people who are male, 60+ old , have been taking the drug for < 1 month, also take medication Lasix, and have Atrial fibrillation/flutter. This study is created by eHealthMe based on reports of 1,216 people who have side effects when taking Dantrium 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.
1,216 people reported to have side effects when taking Dantrium.
Among them, 15 people (1.23%) have Slow rhr
Number of reports submitted per year:
Time on Dantrium when people have Slow rhr *:
- < 1 month: 57.14 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 42.86 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
Gender of people who have Slow rhr when taking Dantrium *:
- female: 20 %
- male: 80 %
Age of people who have Slow rhr when taking Dantrium *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 20.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 13.33 %
- 60+: 66.67 %
Top conditions involved for these people *:
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 5 people, 33.33%
- Itching: 4 people, 26.67%
- Constipation: 4 people, 26.67%
- Renal Failure Chronic (long lasting kidney dysfunction): 4 people, 26.67%
- High Blood Pressure: 4 people, 26.67%
Top co-used drugs for these people *:
- Allegra: 4 people, 26.67%
- Lasix: 4 people, 26.67%
- Allopurinol: 3 people, 20.00%
- Tegretol: 3 people, 20.00%
- Diovan: 3 people, 20.00%
Top other side effects for these people *:
- Pneumonia: 4 people, 26.67%
- Blood Creatinine Increased: 4 people, 26.67%
- Hypotension (abnormally low blood pressure): 4 people, 26.67%
- Urine Output - Decreased: 3 people, 20.00%
- Drug Level Increased: 3 people, 20.00%
* Approximation only. Some reports may have incomplete information.
FDA reports used in this study
- Want to find out more about the FDA reports used in the study? You can request them from FDA.
Do you have Slow rhr while taking Dantrium?
You are not alone:
Dantrium has active ingredients of dantrolene sodium. (latest outcomes from Dantrium 1,227 users)
Slow rhr has been reported by people with high blood pressure, atrial fibrillation/flutter, multiple sclerosis, depression, pain (latest reports from 35,112 Slow rhr patients).
Drugs that are associated with Slow rhrSlow rhr (2,312 drugs)
Could your condition cause Slow rhrSlow rhr (1,299 conditions)
Dantrium side effects
- Dantrium side effects (1,216 reports)
Browse all side effects of Dantriuma 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
- Contac and Dyrenium drug interaction - now
- Nuplazid and Keppra drug interaction - now
- Opdivo and Warfarin Sodium drug interaction - a second ago
- Metoprolol Tartrate and Ventolin drug interaction - 8 seconds ago
- Will you have Urticaria with High Blood Cholesterol? - 8 seconds ago
Recent personal studies
- A study for a 46 year old woman who takes Ambien, Probiotic, Nexium, Xanax - 2 hours ago
- A study for a 39 year old woman who takes Zoloft, Metformin - 3 hours ago
- A study for a 21 year old woman who takes Celexa, Concerta - 5 hours ago
- A study for a 20 year old woman who takes Retin-a - 5 hours ago
- A study for a 79 year old woman who takes Zocor, Garlic, Profen, Aspirin - 6 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.