Ofloxacin and Para drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Ofloxacin (ofloxacin) and Para (para - aminobenzoic acid (paba)). Common drug interactions include drug-induced liver injury among females and multiple-drug resistance among males.

The phase IV clinical study analyzes what interactions people have when they take Ofloxacin and Para. It is created by eHealthMe based on reports of 40 people who take the same drugs from the FDA, and is updated regularly.

What is Ofloxacin?

Ofloxacin has active ingredients of ofloxacin. It is often used in urinary tract infection. eHealthMe is studying from 9,372 Ofloxacin users. Check the latest studies of Ofloxacin.

What is Para?

Para has active ingredients of para - aminobenzoic acid (paba). eHealthMe is studying from 2,194 Para users. Check the latest studies of Para.



On Jul, 15, 2026

40 people who take Ofloxacin and Para together, and have interactions are studied.

Ofloxacin and Para drug interactions.

What are the common drug interactions of Ofloxacin and Para, by gender? *:

female:

  1. Drug-induced liver injury (diseases of the liver that are caused by physician-prescribed medications)
  2. Hepatosplenomegaly (enlargement of both the liver and the spleen)
  3. Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)
  4. Pallor
  5. Abdominal distension
  6. Neuropathy peripheral (surface nerve damage)
  7. Respiratory failure (inadequate gas exchange by the respiratory system)
  8. Bacterial infection
  9. Capillary disorder (capillary disease)
  10. Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)

male:

  1. Multiple-drug resistance
  2. Pathogen resistance
  3. Disease recurrence
  4. Tuberculosis (a bacterial infection by mycobacterium tuberculosis)
  5. Drug resistance (reduction in effectiveness of a drug)

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

0-1:

n/a

2-9:

  1. Alanine aminotransferase increased
  2. Anaemia (lack of blood)
  3. Drug-induced liver injury (diseases of the liver that are caused by physician-prescribed medications)
  4. Gastrointestinal disorder (functional problems of gastrointestinal tract)
  5. Hepatosplenomegaly (enlargement of both the liver and the spleen)
  6. Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)
  7. Pallor
  8. Abdominal distension
  9. Drug resistance (reduction in effectiveness of a drug)
  10. Ataxia (loss of full control of bodily movements)

10-19:

  1. Drug resistance (reduction in effectiveness of a drug)
  2. Anaemia (lack of blood)
  3. Neuropathy peripheral (surface nerve damage)
  4. Drug ineffective
  5. Leukopenia (less number of white blood cells in blood)
  6. Blood thyroid stimulating hormone increased
  7. Hypoaesthesia (reduced sense of touch or sensation)
  8. Multiple-drug resistance
  9. Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect)
  10. Respiratory failure (inadequate gas exchange by the respiratory system)

20-29:

  1. Drug resistance (reduction in effectiveness of a drug)
  2. Gastrointestinal disorder (functional problems of gastrointestinal tract)
  3. Pathogen resistance

30-39:

  1. Drug ineffective
  2. Anaemia (lack of blood)
  3. Bacterial infection
  4. Capillary disorder (capillary disease)
  5. Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
  6. Hypertensive crisis
  7. Nephropathy toxic (damage to kidney due to toxins)
  8. Pulmonary haemorrhage (acute bleeding from the lung)
  9. Respiratory failure (inadequate gas exchange by the respiratory system)
  10. Sinus tachycardia (a heart rhythm with elevated rate of impulses originating from the sinoatrial node)

40-49:

  1. Multiple-drug resistance
  2. Arthralgia (joint pain)

50-59:

  1. Drug resistance (reduction in effectiveness of a drug)

60+:

  1. Delirium (wild excitement)
  2. Diarrhoea
  3. Dysarthria (speech disorder)
  4. Hallucination, visual (seeing things that aren't there)
  5. Hypovolaemic shock (shock caused by severe blood or fluid loss)
  6. Sleep disorder
  7. Social avoidant behaviour (avoiding social connection a personality disorder)
  8. Unresponsive to stimuli

What are the existing conditions these people have? *

  1. Tuberculosis (a bacterial infection by mycobacterium tuberculosis): 27 people, 67.50%
  2. Pulmonary Tuberculosis (lungs tuberculosis): 10 people, 25.00%
  3. Meningitis Tuberculous (a bacterial infection of the membranes covering the brain and spinal cord (meninges)): 4 people, 10.00%
  4. Disseminated Tuberculosis: 2 people, 5.00%
  5. Delirium (wild excitement): 2 people, 5.00%

* Approximation only. Some reports may have incomplete information.

Do you take Ofloxacin and Para?

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Related studies:

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

Browse all drug interactions of Ofloxacin and Para:

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 Ofloxacin:

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 Para:

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 Ofloxacin 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 Para 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 ofloxacin and para - aminobenzoic acid (paba) (the active ingredients of Ofloxacin and Para, respectively), and Ofloxacin and Para (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.

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