Ddavp and Zoloft drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Ddavp (desmopressin acetate) and Zoloft (sertraline hydrochloride). Common drug interactions include gastrointestinal disorder among females and injury among males.

The phase IV clinical study analyzes what interactions people have when they take Ddavp and Zoloft. It is created by eHealthMe based on reports of 54 people who take the same drugs from the FDA, and is updated regularly.

What is Ddavp?

Ddavp has active ingredients of desmopressin acetate. It is often used in diabetes insipidus. eHealthMe is studying from 2,614 Ddavp users. Check the latest studies of Ddavp.

What is Zoloft?

Zoloft has active ingredients of sertraline hydrochloride. It is often used in depression. eHealthMe is studying from 138,798 Zoloft users. Check the latest studies of Zoloft.



On Aug, 10, 2026

54 people who take Ddavp and Zoloft together, and have interactions are studied.

Ddavp and Zoloft drug interactions.

What are the common drug interactions of Ddavp and Zoloft, by gender? *:

female:

  1. Gastrointestinal disorder (functional problems of gastrointestinal tract)
  2. Headache (pain in head)
  3. Herpes zoster
  4. Pain
  5. Abscess (pus)
  6. Acute sinusitis
  7. Alopecia (absence of hair from areas of the body)
  8. Anaemia (lack of blood)
  9. Arthralgia (joint pain)
  10. Blood calcium decreased

male:

  1. Injury
  2. Drug ineffective
  3. Visual impairment
  4. Chills (felling of cold)
  5. Diarrhoea
  6. Pyrexia (fever)
  7. Sinus tachycardia (a heart rhythm with elevated rate of impulses originating from the sinoatrial node)
  8. Abnormal behaviour
  9. Diabetes mellitus insulin-dependent
  10. Hypersensitivity

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

0-1:

n/a

2-9:

  1. Blood glucose increased
  2. Diabetes mellitus insulin-dependent
  3. Drug ineffective
  4. Nausea (feeling of having an urge to vomit)
  5. Urine ketone body present
  6. Alanine aminotransferase increased
  7. Aphasia (damage to the parts of the brain that control language)
  8. Drooling (drop saliva uncontrollably from the mouth)
  9. Movement disorder (neurological syndromes where they may be excess of movement or a paucity of movement that is not connected to weakness)

10-19:

  1. Hypersensitivity
  2. Respiratory tract infection
  3. Sinusitis (inflammation of sinus)
  4. Abnormal behaviour
  5. Drug ineffective
  6. Urticaria (rash of round, red welts on the skin that itch intensely)
  7. Weight increased
  8. Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
  9. Tardive dyskinesia (a disorder that involves involuntary movements)
  10. Aggression

20-29:

  1. Abdominal pain
  2. Acute abdomen
  3. Convulsions (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled of muscles contract and relax rapidly and repeatedly)
  4. Gastrointestinal disorder (functional problems of gastrointestinal tract)
  5. Grand mal convulsion (a type of generalized seizure that affects the entire brain)

30-39:

  1. Decreased appetite
  2. Fall
  3. Uterine atony (failure of the uterus to contract following delivery)

40-49:

  1. Headache (pain in head)
  2. Herpes zoster
  3. Abscess (pus)
  4. Acute sinusitis
  5. Alopecia (absence of hair from areas of the body)
  6. Anaemia (lack of blood)
  7. Arthralgia (joint pain)
  8. Blood calcium decreased
  9. Bone cyst
  10. Bone disorder

50-59:

  1. Mood altered (changes in mood)
  2. Temporomandibular joint syndrome (pain at the temporomandibular joint due to various causes of increased muscle tension and spasm. it is believed that syndrome is a physical manifestation of psychological stress)
  3. Tendon pain
  4. Tongue injury
  5. Visual impairment
  6. Dyspepsia (indigestion)
  7. Dyspnoea (difficult or laboured respiration)
  8. Pain
  9. Abscess (pus)
  10. Acute sinusitis

60+:

  1. Abdominal pain
  2. Asthenia (weakness)
  3. Diarrhoea
  4. Dysstasia (difficulty in standing)
  5. Malaise (a feeling of general discomfort or uneasiness)
  6. Heart rate increased
  7. Sinus tachycardia (a heart rhythm with elevated rate of impulses originating from the sinoatrial node)
  8. Skin cancer

What are the existing conditions these people have? *

  1. Pain: 6 people, 11.11%
  2. Insomnia (sleeplessness): 6 people, 11.11%
  3. Bipolar Disorder (mood disorder): 6 people, 11.11%
  4. Bedwetting: 6 people, 11.11%
  5. Nausea And Vomiting: 4 people, 7.41%
  6. Nausea (feeling of having an urge to vomit): 4 people, 7.41%
  7. Multiple Myeloma (cancer of the plasma cells): 4 people, 7.41%
  8. Growth Hormone Deficiency: 4 people, 7.41%
  9. Anaemia (lack of blood): 4 people, 7.41%
  10. Stress And Anxiety: 3 people, 5.56%

* Approximation only. Some reports may have incomplete information.

Do you take Ddavp and Zoloft?

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Related studies:

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

Browse all drug interactions of Ddavp and Zoloft:

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 Ddavp:

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 Zoloft:

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 Ddavp 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 Zoloft 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

Related publications that referenced our studies


How the study uses the data?

The study uses data from the FDA. It is based on desmopressin acetate and sertraline hydrochloride (the active ingredients of Ddavp and Zoloft, respectively), and Ddavp and Zoloft (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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