Sumatriptan and Ibrance drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Sumatriptan (sumatriptan succinate) and Ibrance (palbociclib). Common drug interactions include fatigue among females.
The phase IV clinical study analyzes what interactions people have when they take Sumatriptan and Ibrance. It is created by eHealthMe based on reports of 51 people who take the same drugs from the FDA, and is updated regularly.
What is Sumatriptan?
Sumatriptan has active ingredients of sumatriptan succinate. It is often used in migraine. eHealthMe is studying from 18,159 Sumatriptan users. Check the latest studies of Sumatriptan.
What is Ibrance?
Ibrance has active ingredients of palbociclib. eHealthMe is studying from 104,434 Ibrance users. Check the latest studies of Ibrance.
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 >>>.
51 people who take Sumatriptan and Ibrance together, and have interactions are studied.

What are the common drug interactions of Sumatriptan and Ibrance, by gender? *:
female:
- Fatigue (feeling of tiredness)
- White blood cell count decreased
- Dry skin
- Dyspnoea (difficult or laboured respiration)
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Rash
- Tumour marker increased
- Breast cancer metastatic
- Malignant neoplasm progression (cancer tumour came back)
- Lacrimation increased
male:
n/a
What are the common drug interactions of Sumatriptan and Ibrance, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Disease progression
40-49:
- Rash
- Fatigue (feeling of tiredness)
- Diarrhoea
- White blood cell count decreased
- Alopecia (absence of hair from areas of the body)
- Eyelid ptosis (falling of the upper or lower eyelid)
- Hallucination, auditory (perceiving sounds without auditory stimulus)
- Hypotension (abnormally low blood pressure)
- Lacrimation increased
- Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
50-59:
- Oxygen saturation decreased
- Postmenopausal haemorrhage (post-menopausal bleeding)
- Pyrexia (fever)
- Rash
- Tongue coated
- Weight increased
- Fatigue (feeling of tiredness)
- White blood cell count decreased
- Alopecia (absence of hair from areas of the body)
- Back pain
60+:
- Fatigue (feeling of tiredness)
- Thrombocytopenia (decrease of platelets in blood)
- Diarrhoea
- Injection site discomfort
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Palmar-plantar erythrodysaesthesia syndrome (hand-foot syndrome)
- Skin exfoliation (removal of the oldest dead skin cells)
- Tumour marker increased
- Vomiting
- White blood cell count decreased
What are the existing conditions these people have? *
- Breast Cancer Female: 16 people, 31.37%
- Breast Cancer Metastatic: 11 people, 21.57%
- Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 10 people, 19.61%
- High Blood Pressure: 10 people, 19.61%
- Breast Cancer: 7 people, 13.73%
- Pain: 3 people, 5.88%
- Metastases To Breast (cancer spreads to brain): 3 people, 5.88%
* Approximation only. Some reports may have incomplete information.
Do you take Sumatriptan and Ibrance?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Sumatriptan (18,159 reports)
- Ibrance (104,434 reports)
Browse all drug interactions of Sumatriptan and Ibrance:
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 Sumatriptan:
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 Ibrance:
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 Sumatriptan 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 Ibrance 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 zHow the study uses the data?
The study uses data from the FDA. It is based on sumatriptan succinate and palbociclib (the active ingredients of Sumatriptan and Ibrance, respectively), and Sumatriptan and Ibrance (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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