Citalopram hydrobromide and Atripla drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Citalopram hydrobromide (citalopram hydrobromide) and Atripla (efavirenz; emtricitabine; tenofovir disoproxil fumarate). Common drug interactions include abscess among females and emotional distress among males.
The phase IV clinical study analyzes what interactions people have when they take Citalopram hydrobromide and Atripla. It is created by eHealthMe based on reports of 22 people who take the same drugs from the FDA, and is updated regularly.
What is Citalopram hydrobromide?
Citalopram hydrobromide has active ingredients of citalopram hydrobromide. It is often used in depression. eHealthMe is studying from 36,878 Citalopram hydrobromide users. Check the latest studies of Citalopram hydrobromide.
What is Atripla?
Atripla has active ingredients of efavirenz; emtricitabine; tenofovir disoproxil fumarate. It is often used in hiv infection. eHealthMe is studying from 36,036 Atripla users. Check the latest studies of Atripla.
22 people who take Citalopram hydrobromide and Atripla together, and have interactions are studied.

What are the common drug interactions of Citalopram Hydrobromide and Atripla, by gender? *:
female:
- Abscess (pus)
- Anaemia (lack of blood)
- Arthralgia (joint pain)
- Bone marrow failure
- Deep vein thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis)
- Disease progression
- Drug ineffective
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
male:
- Emotional distress
- Pain
- Osteonecrosis (death of bone)
- Tooth loss
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Blood alkaline phosphatase increased
- Blood bilirubin increased
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Fatigue (feeling of tiredness)
What are the common drug interactions of Citalopram Hydrobromide and Atripla, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Fatigue (feeling of tiredness)
- Memory impairment
- Middle insomnia (difficulty returning to sleep after awakening either in the middle of the night)
- Nervousness
- Road traffic accident
- Somnolence (a state of near-sleep, a strong desire for sleep)
30-39:
- Emotional distress
- Pain
- Bone density decreased
- Osteonecrosis (death of bone)
- Tooth loss
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Chronic kidney disease
- Nephropathy (damage to or disease of a kidney)
- Overdose
- Pulmonary arterial hypertension (high blood pressure in the arteries of lungs)
40-49:
- Abscess (pus)
- Neutropenia (an abnormally low number of neutrophils)
- Small intestinal obstruction (blockage in small intestine)
50-59:
- Bone density decreased
- Emotional distress
- Pain
- Osteonecrosis (death of bone)
- Tooth loss
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Chronic kidney disease
- Disease progression
- Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
- Infection
60+:
- Gallbladder disorder
- Haemorrhage (bleeding)
- Chronic kidney disease
- Emotional distress
- Pain
- Weight decreased
- Ill-defined disorder
- Insulin-like growth factor increased
- Alanine aminotransferase increased
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
What are the existing conditions these people have? *
- Stress And Anxiety: 7 people, 31.82%
- High Blood Pressure: 7 people, 31.82%
- Urinary Tract Infection: 5 people, 22.73%
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 5 people, 22.73%
- Respiratory Tract Irritation: 4 people, 18.18%
- Pain: 4 people, 18.18%
- Neuralgia (pain in one or more nerves): 4 people, 18.18%
- Infection: 3 people, 13.64%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 13.64%
- Pneumonia: 2 people, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Citalopram hydrobromide and Atripla?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Citalopram hydrobromide (36,878 reports)
- Atripla (36,036 reports)
Browse all drug interactions of Citalopram hydrobromide and Atripla:
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 Citalopram hydrobromide:
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 Atripla:
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 Citalopram hydrobromide 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 Atripla 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
- Hosseini, S. H., & Ahmadi, A., "Peripheral edema occurring during treatment with risperidone combined with citalopram", Case reports in medicine, 2012 Jan .
- Hosseini, S. H., & Ahmadi, A., "Peripheral edema occurring during treatment with risperidone combined with citalopram", Case reports in medicine, 2012 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on citalopram hydrobromide and efavirenz; emtricitabine; tenofovir disoproxil fumarate (the active ingredients of Citalopram hydrobromide and Atripla, respectively), and Citalopram hydrobromide and Atripla (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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