Alendronate sodium and Hyperamylasaemia - a phase IV clinical study of FDA data
Hyperamylasaemia is found among people who take Alendronate sodium, especially for people who are female, 60+ old.
The phase IV clinical study analyzes which people take Alendronate sodium and have Hyperamylasaemia. It is created by eHealthMe based on reports of 40,203 people who have side effects when taking Alendronate sodium from the FDA, and is updated regularly. You can use the study as a second opinion to make health care decisions.
Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 600+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.
40,203 people reported to have side effects when taking Alendronate sodium.
Among them, 6 people (0.01%) have Hyperamylasaemia.
What is Alendronate sodium?
Alendronate sodium has active ingredients of alendronate sodium. It is often used in osteoporosis. eHealthMe is studying from 40,879 Alendronate sodium users for its effectiveness, alternative drugs and more.
What is Hyperamylasaemia?
Hyperamylasaemia (acute pancreatitis in which serum amylase is usually elevated more than 4-fold) is found to be associated with 397 drugs and 238 conditions by eHealthMe.
Number of Alendronate sodium and Hyperamylasaemia reports submitted per year:
Gender of people who have Hyperamylasaemia when taking Alendronate sodium *:
- female: 100 %
- male: 0.0 %
Age of people who have Hyperamylasaemia when taking Alendronate sodium *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 33.33 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 66.67 %
Common drugs people take besides Alendronate sodium *:
- Allopurinol: 6 people, 100.00%
- Prednisolone: 6 people, 100.00%
- Zometa: 4 people, 66.67%
- Velcade: 4 people, 66.67%
- Nizatidine: 4 people, 66.67%
- Lasix: 4 people, 66.67%
- Diflucan: 3 people, 50.00%
- Zyrtec: 2 people, 33.33%
- Levofloxacin: 2 people, 33.33%
- Chlorhexidine Gluconate: 2 people, 33.33%
Common side effects people have besides Hyperamylasaemia *:
- Hyperglycemia (high blood sugar): 4 people, 66.67%
- Anaemia (lack of blood): 4 people, 66.67%
- Disease Progression: 4 people, 66.67%
- Respiratory Acidosis (respiratory failure or ventilatory failure, causes the ph of blood and other bodily fluids to decrease): 4 people, 66.67%
- Hypercalcaemia (elevated calcium (ca+) level in the blood): 4 people, 66.67%
- Pulmonary Infarction (death of a small area of lung): 4 people, 66.67%
- Thrombocytopenia (decrease of platelets in blood): 4 people, 66.67%
- Hyperkalemia (damage to or disease of the kidney): 4 people, 66.67%
- Hyperuricaemia (level of uric acid in the blood that is abnormally high): 4 people, 66.67%
- Deep Venous Thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis): 4 people, 66.67%
Common conditions people have *:
- Multiple Myeloma (cancer of the plasma cells): 4 people, 66.67%
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes): 4 people, 66.67%
- Iron Overload: 2 people, 33.33%
- Aplastic Anemia: 2 people, 33.33%
* Approximation only. Some reports may have incomplete information.
Do you take Alendronate sodium and have Hyperamylasaemia?Check whether Hyperamylasaemia is associated with a drug or a condition
How to use the study?
You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.
Related publications that referenced our studies
- Stuckey BG, Sallie R, "Alendronate-induced unmasking or deterioration of coeliac disease: a case series", Osteoporosis International, 2015 Jan .
- Lee WY, Sun LM, Lin MC, Liang JA, Chang SN, Sung FC, Muo CH, Kao CH, "A higher dosage of oral alendronate will increase the subsequent cancer risk of osteoporosis patients in Taiwan: a population-based cohort study", PloS one, 2012 Dec .
How severe was Hyperamylasaemia and when was it recovered:
Expand to all the drugs that have ingredients of alendronate sodium:
Alternative drugs to, pros and cons of Alendronate sodium:
- Alendronate sodium (40,879 reports)
Common Alendronate sodium side effects:
- Fatigue (feeling of tiredness): 6,004 reports
- Pain: 5,043 reports
- Drug ineffective: 4,933 reports
- Joint pain: 4,792 reports
- Rashes (redness): 4,063 reports
- High blood pressure: 3,988 reports
Browse all side effects of Alendronate sodium: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 z
Hyperamylasaemia treatments and more:
- Hyperamylasaemia (710 reports)
COVID vaccines that are related to Hyperamylasaemia:
- Hyperamylasaemia in Moderna COVID Vaccine
- Hyperamylasaemia in Pfizer BioNTech Covid Vaccine
- Hyperamylasaemia in Johnson and Johnson Covid Vaccine
All the drugs that are associated with Hyperamylasaemia:
- Hyperamylasaemia (397 drugs)
All the conditions that are associated with Hyperamylasaemia:
- Hyperamylasaemia (238 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on alendronate sodium (the active ingredients of Alendronate sodium) and Alendronate sodium (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.
Who is eHealthMe?
With medical big data and proven AI 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 600+ 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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