Ocrevus and Atarax drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Ocrevus (ocrelizumab) and Atarax (hydroxyzine hydrochloride). Common drug interactions include headache among females and chest discomfort among males.
The phase IV clinical study analyzes what interactions people have when they take Ocrevus and Atarax. It is created by eHealthMe based on reports of 37 people who take the same drugs from the FDA, and is updated regularly.
What is Ocrevus?
Ocrevus has active ingredients of ocrelizumab. eHealthMe is studying from 56,583 Ocrevus users. Check the latest studies of Ocrevus.
What is Atarax?
Atarax has active ingredients of hydroxyzine hydrochloride. It is often used in stress and anxiety. eHealthMe is studying from 23,553 Atarax users. Check the latest studies of Atarax.
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 >>>.
37 people who take Ocrevus and Atarax together, and have interactions are studied.

What are the common drug interactions of Ocrevus and Atarax, by gender? *:
female:
- Headache (pain in head)
- Oropharyngeal pain
- Infusion related reaction
- Fatigue (feeling of tiredness)
- Drug ineffective
- Gait disturbance
- Pyrexia (fever)
- Dizziness
- Feeling hot
- Multiple sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath)
male:
- Chest discomfort
- Depression
- Fatigue (feeling of tiredness)
- Fungal infection
- Immunosuppression
- Infusion related reaction
- Pain in extremity
- Rash
What are the common drug interactions of Ocrevus and Atarax, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Oropharyngeal pain
- Throat irritation
30-39:
- Fatigue (feeling of tiredness)
- Abdominal pain
- Alopecia (absence of hair from areas of the body)
- Back pain
- Diarrhoea
- Dyspepsia (indigestion)
- Haemorrhoids (a swollen vein or group of veins in the region of the anus)
- Nausea (feeling of having an urge to vomit)
- Polyp
- Chest discomfort
40-49:
- Serratia infection (bacterial infection)
- Sputum discoloured
- Weight increased
- Asthenia (weakness)
- Infusion related reaction
- Oropharyngeal pain
- Back pain
- Headache (pain in head)
- Gait disturbance
- Dizziness
50-59:
- Fatigue (feeling of tiredness)
- Headache (pain in head)
- Heart rate increased
- Herpes zoster
- Skin infection
- Urticaria (rash of round, red welts on the skin that itch intensely)
- Weight increased
- Chills (felling of cold)
- Dry mouth
- Dyspnoea (difficult or laboured respiration)
60+:
- Cough
- Heart rate increased
- Lethargy (tiredness)
- Oxygen saturation decreased
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
- Respiratory distress (difficulty in breathing)
- Septic shock (shock due to blood infection)
- Toxic encephalopathy (a degenerative neurologic disorder caused by exposure to toxic substances)
- Urinary tract infection
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): 20 people, 54.05%
- Urinary Tract Infection: 6 people, 16.22%
- Pain: 5 people, 13.51%
- Restless Leg Syndrome (a powerful urge to move your legs): 4 people, 10.81%
- 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, 10.81%
- Hypoaesthesia (reduced sense of touch or sensation): 4 people, 10.81%
- Eczema (patches of skin become rough and inflamed, with itching and bleeding blisters): 4 people, 10.81%
- Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 3 people, 8.11%
- Seasonal Allergy (allergic condition due to certain season): 2 people, 5.41%
- Progressive Multiple Sclerosis (chronic autoimmune disease of the central nervous system in which gradual destruction of myelin occurs in patches throughout the brain or spinal cord): 2 people, 5.41%
* Approximation only. Some reports may have incomplete information.
Do you take Ocrevus and Atarax?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Ocrevus and Atarax:
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 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 side effects of Atarax:
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 zBrowse all interactions between Atarax 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
- Ate? ?, Arikan MF, Kaplan M, Altay M, "Hydroxyzine induced pancytopenia and petechial rashes: a rare complication", Journal Of Contemporary Medicine, 2017 Jan .
- Ate? ?, Arikan MF, Kaplan M, Altay M, "Hydroxyzine induced pancytopenia and petechial rashes: a rare complication", Journal Of Contemporary Medicine, 2017 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on ocrelizumab and hydroxyzine hydrochloride (the active ingredients of Ocrevus and Atarax, respectively), and Ocrevus and Atarax (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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