Humalog and Ipf - a phase IV clinical study of FDA data
Summary:
Ipf is reported as a side effect among people who take Humalog (insulin lispro recombinant), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Lantus, and have High blood pressure.
The phase IV clinical study analyzes which people have Ipf when taking Humalog. It is created by eHealthMe based on reports of 136,521 people who have side effects when taking Humalog from the FDA, and is updated regularly.
What is Humalog?
Humalog has active ingredients of insulin lispro recombinant. It is often used in diabetes. eHealthMe is studying from 137,126 Humalog users. Check the latest studies of Humalog.
What is Ipf?
Ipf is found to be associated with 1,933 drugs and 2,253 conditions by eHealthMe. Check the latest studies of Ipf.
136,521 people reported to have side effects when taking Humalog.
Among them, 120 people (0.09%) have Ipf.

Among these 120 people:
How long have people been on Humalog when they have Ipf? *
What is the gender of people who have Ipf when taking Humalog? *
What is the age of people who have Ipf when taking Humalog? *
What are other drugs people take besides Humalog? *
What are other side effects people have besides Ipf? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Humalog and have Ipf?
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Related studies:
Effectiveness of, long term effects of, and alternative drugs to Humalog:
- Humalog (137,126 reports)
Ipf treatments and more:
- Ipf (79,192 reports)
How severe was Ipf and when was it recovered:
Expand to all the drugs that have ingredients of insulin lispro recombinant:
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+
Common Humalog side effects:
- Humalog side effect: Blood glucose increased (38,656 reports)
- Humalog side effect: Blood glucose decreased (9,765 reports)
- Humalog side effect: Visual impairment (4,919 reports)
- Humalog side effect: Malaise (a feeling of general discomfort or uneasiness) (4,407 reports)
Browse all side effects of Humalog:
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 zCommon drugs associated with Ipf:
- Methotrexate side effect: Ipf (4,714 reports)
- Prednisone side effect: Ipf (4,117 reports)
- Humira side effect: Ipf (2,869 reports)
- Enbrel side effect: Ipf (2,842 reports)
- Ofev side effect: Ipf (2,063 reports)
- Remicade side effect: Ipf (2,043 reports)
- Actemra side effect: Ipf (2,024 reports)
- Leflunomide side effect: Ipf (1,957 reports)
- Xeljanz side effect: Ipf (1,940 reports)
- Pantoprazole side effect: Ipf (1,758 reports)
Browse all the drugs that are associated with Ipf:
- Ipf (1,932 drugs)
Common conditions associated with Ipf:
- Ra: 5,843 reports
- Ipf: 2,256 reports
- Atrial fibrillation/flutter: 1,089 reports
- Hypertension aggravated: 1,023 reports
- Blood pressure increased: 1,015 reports
- Psoriatic arthropathy: 851 reports
- Idiopathic pulmonary fibrosis: 843 reports
- Primary pulmonary hypertension: 793 reports
- Psoriasis: 789 reports
- Osteoporosis: 682 reports
Browse all the conditions that are associated with Ipf:
- Ipf (2,253 conditions)
Drugs similar to Humalog and Ipf :
- Actos side effect: Ipf
- Byetta side effect: Ipf
- Glimepiride side effect: Ipf
- Glipizide side effect: Ipf
- Glucophage side effect: Ipf
- Glyburide side effect: Ipf
- Insulin side effect: Ipf
- Janumet side effect: Ipf
- Januvia side effect: Ipf
- Lantus side effect: Ipf
- Levemir side effect: Ipf
- Metformin side effect: Ipf
- Metformin hydrochloride side effect: Ipf
- Novolog side effect: Ipf
- Victoza side effect: Ipf
How the study uses the data?
The study uses data from the FDA. It is based on insulin lispro recombinant (the active ingredients of Humalog) and Humalog (the brand name). 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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