Precose and Fosamax drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Precose (acarbose) and Fosamax (alendronate sodium). Common drug interactions include femur fracture among females and haematoma among males.
The phase IV clinical study analyzes what interactions people have when they take Precose and Fosamax. It is created by eHealthMe based on reports of 18 people who take the same drugs from the FDA, and is updated regularly.
What is Precose?
Precose has active ingredients of acarbose. eHealthMe is studying from 1,189 Precose users. Check the latest studies of Precose.
What is Fosamax?
Fosamax has active ingredients of alendronate sodium. It is often used in osteoporosis. eHealthMe is studying from 105,452 Fosamax users. Check the latest studies of Fosamax.
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 >>>.
18 people who take Precose and Fosamax together, and have interactions are studied.

What are the common drug interactions of Precose and Fosamax, 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)
- Asthma
- Bone disorder
- Fracture displacement
- Fracture nonunion (permanent failure of healing following a broken bone)
- Groin pain
- Mobility decreased (ability to move is reduced)
male:
- Haematoma (collection of blood outside the blood vessels)
- Arthralgia (joint pain)
- Fracture displacement
- Fracture nonunion (permanent failure of healing following a broken bone)
- Groin pain
- Low turnover osteopathy (slow removal of old bone and its replacement by new bone)
- Mass
- Mobility decreased (ability to move is reduced)
- Monoparesis (one limb is very weak, but not completely paralyzed)
- Muscle injury
What are the common drug interactions of Precose and Fosamax, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Arthralgia (joint pain)
- Bone disorder
- Dysstasia (difficulty in standing)
- Femur fracture
- 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)
40-49:
n/a
50-59:
- 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)
60+:
- Weight increased
- Accident
- Injection site bruising
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Nausea (feeling of having an urge to vomit)
- Pruritus generalised (generalized itching)
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Therapeutic response unexpected
- Thinking abnormal
- Tooth abscess (pus formation in tooth)
What are the existing conditions these people have? *
- Asthma: 4 people, 22.22%
- Diabetes: 2 people, 11.11%
- Type 2 Diabetes: 1 person, 5.56%
- Hyperlipidaemia (presence of excess lipids in the blood): 1 person, 5.56%
- High Blood Pressure: 1 person, 5.56%
- High Blood Cholesterol: 1 person, 5.56%
- 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): 1 person, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Precose and Fosamax?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Precose and Fosamax:
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 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 side effects of Fosamax:
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 zBrowse all interactions between Fosamax 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
- 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 .
- 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 the study uses the data?
The study uses data from the FDA. It is based on acarbose and alendronate sodium (the active ingredients of Precose and Fosamax, respectively), and Precose and Fosamax (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.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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