Who have Dacryoadenitis acquired with Tecfidera - from FDA reports
Dacryoadenitis acquired is reported only by a few people who take Tecfidera. We study 84,093 people who have side effects while taking Tecfidera from FDA. Among them, 1 have Dacryoadenitis acquired. Find out below who they are, when they have Dacryoadenitis acquired and more.
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84,093 people reported to have side effects when taking Tecfidera.
Among them, 1 person (0.0%) has Dacryoadenitis acquired
Number of reports submitted per year:
Gender of people who have Dacryoadenitis acquired when taking Tecfidera *:
- female: 100 %
- male: 0.0 %
Age of people who have Dacryoadenitis acquired when taking Tecfidera *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 100 %
- 60+: 0.0 %
Top co-used drugs for these people *:
- Tysabri: 1 person, 100.00%
Top other side effects for these people *:
- Urinary Tract Infection: 1 person, 100.00%
- Fatigue (feeling of tiredness): 1 person, 100.00%
* Approximation only. Some reports may have incomplete information.
Do you have Dacryoadenitis acquired while taking Tecfidera?
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Related studies
Tecfidera
Tecfidera has active ingredients of dimethyl fumarate. It is often used in multiple sclerosis. (latest outcomes from Tecfidera 84,250 users)
Dacryoadenitis acquired
Dacryoadenitis acquired (inflammation of the lacrimal glands acquired) has been reported by people with high blood pressure, hyperthyroidism, hepatitis c, rheumatoid arthritis, multiple sclerosis (latest reports from 35 Dacryoadenitis acquired patients).
Drugs that are associated with Dacryoadenitis acquired
Dacryoadenitis acquired (27 drugs)Could your condition cause Dacryoadenitis acquired
Dacryoadenitis acquired (21 conditions)Tecfidera side effects
- Tecfidera side effects (84,127 reports)
Browse 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 Tecfidera
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 zCompare Tecfidera to similar drugs:
What would happen?
FDA reports used in this study
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