Loraz and Optimark drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Loraz (lorazepam) and Optimark (gadoversetamide). Common drug interactions include injury among females and nephrogenic systemic fibrosis among males.

The phase IV clinical study analyzes what interactions people have when they take Loraz and Optimark. 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 Loraz?

Loraz has active ingredients of lorazepam. It is often used in stress and anxiety. eHealthMe is studying from 165,694 Loraz users. Check the latest studies of Loraz.

What is Optimark?

Optimark has active ingredients of gadoversetamide. eHealthMe is studying from 3,055 Optimark users. Check the latest studies of Optimark.



On Jul, 15, 2026

24 people who take Loraz and Optimark together, and have interactions are studied.

Loraz and Optimark drug interactions.

What are the common drug interactions of Loraz and Optimark, by gender? *:

female:

  1. Injury
  2. Joint range of motion decreased (disease of joint movement)
  3. Pruritus (severe itching of the skin)
  4. Skin fibrosis (fibrous tissue formation on skin)
  5. Emotional distress
  6. Skin lesion
  7. Erythema (redness of the skin)
  8. Pain in extremity
  9. Skin burning sensation
  10. Muscular weakness (muscle weakness)

male:

  1. Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
  2. Oedema peripheral (superficial swelling)
  3. Abasia (inability to walk)
  4. Burning sensation
  5. Gait disturbance
  6. Joint contracture (a permanent shortening of a muscle or joint)
  7. Joint range of motion decreased (disease of joint movement)
  8. Joint stiffness
  9. Mobility decreased (ability to move is reduced)
  10. Myocardial fibrosis (a condition in which the heart's muscle cells are impaired)

What are the common drug interactions of Loraz and Optimark, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

  1. Abscess limb (limb infection)
  2. Asthma
  3. Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
  4. Azotaemia (excess of urea or other nitrogenous compounds in the blood)
  5. Blood bilirubin decreased
  6. Breast calcifications (deposits of calcium that can be seen on a mammogram of the breast)
  7. Bronchopneumonia (inflammation of the lungs, arising in the bronchi or bronchioles)
  8. Cardiac failure acute
  9. Carpal tunnel syndrome (nerve compression at wrist results numbness weakness, pain , swelling)
  10. Coagulopathy (blood's ability to clot is impaired)

40-49:

  1. Oedema peripheral (superficial swelling)
  2. Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
  3. Pain
  4. Skin hypertrophy (skin cells enlarges)
  5. Pruritus (severe itching of the skin)
  6. Skin fibrosis (fibrous tissue formation on skin)
  7. Skin induration (an abnormally hard spot or area on the skin)
  8. General physical health deterioration (weak health status)
  9. Skin discolouration (change of skin colour)
  10. Skin lesion

50-59:

  1. Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
  2. Haemorrhoids (a swollen vein or group of veins in the region of the anus)
  3. Hepatitis cholestatic (flow of bile from the liver is slowed or blocked)
  4. Hepatomegaly (abnormal enlargement of the liver)
  5. Hyperparathyroidism (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium)
  6. Hyperphosphataemia (electrolyte disturbance in which there is an abnormally elevated level of phosphate in the blood)
  7. Hypertension (high blood pressure)
  8. Hypertensive heart disease
  9. Hypogonadism (reduction or absence of hormone secretion or other physiological activity of the gonads (testes or ovaries))
  10. Hypokalaemia (low potassium)

60+:

  1. Emotional distress
  2. Injury
  3. Fibrosis (formation of excess fibrous connective tissue in an organ or tissue)
  4. Mitochondrial toxicity (a condition in which the mitochondria of a body's cells become damaged or decline significantly in number;)
  5. Muscle contracture (a permanent shortening of a muscle)
  6. Muscular weakness (muscle weakness)
  7. Nontherapeutic agent urine positive
  8. Oedema peripheral (superficial swelling)
  9. Skin hypertrophy (skin cells enlarges)
  10. Mobility decreased (ability to move is reduced)

What are the existing conditions these people have? *

  1. Nuclear Magnetic Resonance Imaging Brain: 9 people, 37.50%
  2. Nuclear Magnetic Resonance Imaging Abdominal: 3 people, 12.50%
  3. Wound Complication: 2 people, 8.33%
  4. Neuralgia (pain in one or more nerves): 2 people, 8.33%
  5. Insomnia (sleeplessness): 2 people, 8.33%
  6. Anaemia (lack of blood): 2 people, 8.33%

* Approximation only. Some reports may have incomplete information.

Do you take Loraz and Optimark?

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Loraz and Optimark:

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 z

Sub-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 Loraz:

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 z

Browse all side effects of Optimark:

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 z

Browse all interactions between Loraz 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 z

Browse all interactions between Optimark 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 z

How the study uses the data?

The study uses data from the FDA. It is based on lorazepam and gadoversetamide (the active ingredients of Loraz and Optimark, respectively), and Loraz and Optimark (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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