Krill and Ocrevus drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Krill (krill oil) and Ocrevus (ocrelizumab). Common drug interactions include urinary tract infection among females and multiple sclerosis relapse among males.
The phase IV clinical study analyzes what interactions people have when they take Krill and Ocrevus. It is created by eHealthMe based on reports of 24 people who take the same drugs from the FDA, and is updated regularly.
What is Krill?
Krill has active ingredients of krill oil. It is often used in high blood cholesterol. eHealthMe is studying from 5,404 Krill users. Check the latest studies of Krill.
What is Ocrevus?
Ocrevus has active ingredients of ocrelizumab. eHealthMe is studying from 56,583 Ocrevus users. Check the latest studies of Ocrevus.
24 people who take Krill and Ocrevus together, and have interactions are studied.

What are the common drug interactions of Krill and Ocrevus, by gender? *:
female:
- Urinary tract infection
- Drug ineffective
- Nausea (feeling of having an urge to vomit)
- Breast mass
- Fall
- Pain
- Tremor (trembling or shaking movements in one or more parts of your body)
- Balance disorder
- Gait disturbance
- Muscle spasms (muscle contraction)
male:
- Multiple sclerosis relapse (reoccurrence of a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath)
- Cytokine release syndrome (immediate complication occurring with the use of anti-t cell antibody infusions)
- Muscle spasticity (tight or stiff muscles and an inability to control those muscles)
- Sensory disturbance (sense disturbance)
- Alopecia (absence of hair from areas of the body)
- B-lymphocyte count decreased
- Depression
- Fatigue (feeling of tiredness)
- Infection
- Intervertebral disc protrusion (spinal disc protrusion)
What are the common drug interactions of Krill and Ocrevus, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Sleep disorder
- Spinal pain (pain in spine)
- Stress
- Cytokine release syndrome (immediate complication occurring with the use of anti-t cell antibody infusions)
- Oropharyngeal pain
- Peripheral coldness
- Productive cough
- Aphthous ulcer (mouth ulcer)
- Dry throat
- Gait disturbance
40-49:
n/a
50-59:
- Urinary tract infection
- Nausea (feeling of having an urge to vomit)
- Breast mass
- Drug ineffective
- Balance disorder
- Fall
- Muscle spasms (muscle contraction)
- Neck pain
- Tremor (trembling or shaking movements in one or more parts of your body)
- Anxiety
60+:
- Enteritis infectious (infection with feline parvovirus (fpv), also known as feline panleucopenia virus)
- Multiple sclerosis relapse (reoccurrence of a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath)
- Gait disturbance
- Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
- Hypertension (high blood pressure)
- Hypoaesthesia (reduced sense of touch or sensation)
- Neuralgia (pain in one or more nerves)
- Pain
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Swelling
What are the existing conditions these people have? *
- Relapsing-Remitting Multiple Sclerosis (reoccurrence of an inflammatory disease in which the insulating covers of nerve cells in the brain and spinal cord are damaged): 15 people, 62.50%
- Secondary Progressive Multiple Sclerosis (a stage of ms which comes after relapsing remitting ms in many cases): 4 people, 16.67%
- Primary Progressive Multiple Sclerosis (primary progressive inflammatory disease in which the insulating covers of nerve cells in the brain and spinal cord are damaged): 4 people, 16.67%
- Neuralgia (pain in one or more nerves): 4 people, 16.67%
- Tremor (trembling or shaking movements in one or more parts of your body): 3 people, 12.50%
- Depression: 3 people, 12.50%
- Stress And Anxiety: 2 people, 8.33%
- Pain: 2 people, 8.33%
- Hypersensitivity: 2 people, 8.33%
- High Blood Pressure: 2 people, 8.33%
* Approximation only. Some reports may have incomplete information.
Do you take Krill and Ocrevus?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Krill and Ocrevus:
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 Krill:
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 Ocrevus:
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 Krill 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 Ocrevus 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 krill oil and ocrelizumab (the active ingredients of Krill and Ocrevus, respectively), and Krill and Ocrevus (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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