Keppra and Tukysa drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Keppra (levetiracetam) and Tukysa (tucatinib). Common drug interactions include diarrhoea among females.
The phase IV clinical study analyzes what interactions people have when they take Keppra and Tukysa. It is created by eHealthMe based on reports of 67 people who take the same drugs from the FDA, and is updated regularly.
What is Keppra?
Keppra has active ingredients of levetiracetam. It is often used in epilepsy. eHealthMe is studying from 73,504 Keppra users. Check the latest studies of Keppra.
What is Tukysa?
Tukysa has active ingredients of tucatinib. eHealthMe is studying from 3,216 Tukysa users. Check the latest studies of Tukysa.
67 people who take Keppra and Tukysa together, and have interactions are studied.

What are the common drug interactions of Keppra and Tukysa, by gender? *:
female:
- Diarrhoea
- Confusional state
- Blood potassium decreased
- Photosensitivity reaction
- Skin hypertrophy (skin cells enlarges)
- Memory impairment
- Administration site pain
- Coma (state of unconsciousness lasting more than six hours)
- Constipation
- Hypercapnia (too much smoke)
male:
n/a
What are the common drug interactions of Keppra and Tukysa, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Hypoaesthesia (reduced sense of touch or sensation)
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
- Constipation
- Dizziness
- Fatigue (feeling of tiredness)
- Headache (pain in head)
- Metastasis (spreadable cancer to other organ from origin)
- Erythema (redness of the skin)
- Gait disturbance
40-49:
- Diarrhoea
- Hypokalaemia (low potassium)
- Soft tissue infection
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Fatigue (feeling of tiredness)
- Asthenia (weakness)
- Decreased appetite
- Fall
- Haematocrit decreased
- Haemoglobin decreased
50-59:
- Adverse drug reaction
- Diarrhoea
- Dizziness
- Hepatic enzyme increased
- Joint swelling
- Neuropathy peripheral (surface nerve damage)
- Palmar-plantar erythrodysaesthesia syndrome (hand-foot syndrome)
- Peripheral swelling
- Stomatitis (inflammation of mucous membrane of mouth)
- Fatigue (feeling of tiredness)
60+:
- Confusional state
- Coma (state of unconsciousness lasting more than six hours)
- Hypercapnia (too much smoke)
- Status epilepticus (a life-threatening condition in which the brain is in a state of persistent seizure)
- Catatonia (unresponsive to external stimuli)
- Decreased appetite
- Dysphagia (a condition in which swallowing is difficult or painful)
- Erythema (redness of the skin)
- Fall
- Vomiting
What are the existing conditions these people have? *
- Breast Cancer Female: 23 people, 34.33%
- Osteoporotic Fracture (fracture due to weak bone): 17 people, 25.37%
- Breast Cancer: 15 people, 22.39%
- Diarrhea: 8 people, 11.94%
- Seizures (abnormal excessive or synchronous neuronal activity in the brain): 5 people, 7.46%
- Embolism Venous (embolus may pass into the arterial system): 5 people, 7.46%
* Approximation only. Some reports may have incomplete information.
Do you take Keppra and Tukysa?
- Personalize this study to your gender, age, symptoms and drugs
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Keppra and Tukysa:
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 Keppra:
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 Tukysa:
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 Keppra 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 Tukysa 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
- Schattner A, Al-Bewerat A, "Levetiracetam (Keppra), urinary retention and literature search", A fatty cause of renal failure; what is your diagnosis?, 2016 Oct .
- Spengler DC, Montouris GD, Hohler AD, "Levetiracetam as a possible contributor to acute kidney injury", Clinical therapeutics, 2014 Aug .
- Almeida DM, Jean MR, Chystsiakova A, Monahan E, Oliveira SB, Monteiro IM, "Levetiracetam-associated acute pancreatitis in an adolescent with autism: a case report", Pancreas, 2013 Jan .
- Schattner A, Al-Bewerat A, "Levetiracetam (Keppra), urinary retention and literature search", A fatty cause of renal failure; what is your diagnosis?, 2016 Oct .
- Spengler DC, Montouris GD, Hohler AD, "Levetiracetam as a possible contributor to acute kidney injury", Clinical therapeutics, 2014 Aug .
- Almeida DM, Jean MR, Chystsiakova A, Monahan E, Oliveira SB, Monteiro IM, "Levetiracetam-associated acute pancreatitis in an adolescent with autism: a case report", Pancreas, 2013 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on levetiracetam and tucatinib (the active ingredients of Keppra and Tukysa, respectively), and Keppra and Tukysa (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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