Actonel and Precose drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Actonel (risedronate sodium) and Precose (acarbose). Common drug interactions include femur fracture among females and arthralgia among males.
The phase IV clinical study analyzes what interactions people have when they take Actonel and Precose. It is created by eHealthMe based on reports of 13 people who take the same drugs from the FDA, and is updated regularly.
What is Actonel?
Actonel has active ingredients of risedronate sodium. It is often used in osteoporosis. eHealthMe is studying from 29,369 Actonel users. Check the latest studies of Actonel.
What is Precose?
Precose has active ingredients of acarbose. eHealthMe is studying from 1,189 Precose users. Check the latest studies of Precose.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
13 people who take Actonel and Precose together, and have interactions are studied.

What are the common drug interactions of Actonel and Precose, by gender? *:
female:
- Femur fracture
- Low turnover osteopathy (slow removal of old bone and its replacement by new bone)
- Stress fracture (fracture of a bone caused by repeated (rather than sudden) mechanical stress)
- Arthralgia (joint pain)
- Bone disorder
- Fracture displacement
- Fracture nonunion (permanent failure of healing following a broken bone)
- Groin pain
- Mobility decreased (ability to move is reduced)
- Osteoporotic fracture (fracture due to weak bone)
male:
- Arthralgia (joint pain)
- Femur fracture
- Bone disorder
- Dysstasia (difficulty in standing)
- Fracture delayed union (delayed cure of broken bone)
- Fracture displacement
- Fracture nonunion (permanent failure of healing following a broken bone)
- Groin pain
- Haematoma (collection of blood outside the blood vessels)
- Low turnover osteopathy (slow removal of old bone and its replacement by new bone)
What are the common drug interactions of Actonel and Precose, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Abdominal distension
- Arthralgia (joint pain)
- Back pain
- Bone disorder
- Dehydration (dryness resulting from the removal of water)
- Diarrhoea
- Dysstasia (difficulty in standing)
- Fatigue (feeling of tiredness)
- Femur fracture
- Fracture delayed union (delayed cure of broken bone)
40-49:
- Deep vein thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis)
- Oedema peripheral (superficial swelling)
- Pain in extremity
50-59:
- Groin pain
- Mobility decreased (ability to move is reduced)
- Osteoporotic fracture (fracture due to weak bone)
- Pain
- Pathological fracture (broken bone caused by disease)
- Fall
- Mass
- Staphylococcal infection (an infection with staphylococcus bacteria)
- Hip deformity
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
60+:
- Abdominal pain upper
- Pancreatitis (inflammation of pancreas)
- Renal cyst (kidney cyst)
What are the existing conditions these people have? *
- Bipolar Disorder (mood disorder): 3 people, 23.08%
- Pain: 2 people, 15.38%
- Intracranial Pressure Increased (high pressure inside the skull and thus in the brain tissue and cerebrospinal fluid): 2 people, 15.38%
- Indigestion: 2 people, 15.38%
- Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 2 people, 15.38%
- Hypersensitivity: 2 people, 15.38%
- Glucose Tolerance Impaired (blood glucose is raised beyond normal levels, but not high enough to warrant a diabetes diagnosis): 2 people, 15.38%
- Endocrine Disorder (endocrine diseases are disorders of the endocrine system): 2 people, 15.38%
- Type 2 Diabetes: 1 person, 7.69%
- Csf Test Abnormal: 1 person, 7.69%
* Approximation only. Some reports may have incomplete information.
Do you take Actonel and Precose?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Actonel and Precose:
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 zSub-studies by gender and age:
Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Actonel:
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 zBrowse all side effects of Precose:
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 zBrowse all interactions between Actonel and drugs from A to Z:
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 zBrowse all interactions between Precose and drugs from A to Z:
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 zRelated publications that referenced our studies
- Hirschmann S, Gibel A, Tsvelikhovsky I, Lisker A, "Late-Onset Psychosis and Risedronate Treatment for Osteoporosis: A Case Report", Clinical schizophrenia & related psychoses, 2013 May .
- Ko KD, Cho BL, "Risedronate-related Localized Amnesia in an Elderly Patient with Osteoporosis", Journal of the Korean Geriatrics Society, 2012 Dec .
- Hirschmann S, Gibel A, Tsvelikhovsky I, Lisker A, "Late-Onset Psychosis and Risedronate Treatment for Osteoporosis: A Case Report", Clinical schizophrenia & related psychoses, 2013 May .
- Ko KD, Cho BL, "Risedronate-related Localized Amnesia in an Elderly Patient with Osteoporosis", Journal of the Korean Geriatrics Society, 2012 Dec .
How the study uses the data?
The study uses data from the FDA. It is based on risedronate sodium and acarbose (the active ingredients of Actonel and Precose, respectively), and Actonel and Precose (the brand names). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.
How to use the study?
DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.
Who is eHealthMe?
With medical big data and proven AI/ML 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 800+ peer-reviewed 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.
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