Does FERROUS ANHYDROUS Cause Dyspnoea? 106 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Dyspnoea have been filed in association with FERROUS ANHYDROUS. This represents 21.5% of all adverse event reports for FERROUS ANHYDROUS.
106
Reports of Dyspnoea with FERROUS ANHYDROUS
21.5%
of all FERROUS ANHYDROUS reports
13
Deaths
105
Hospitalizations
How Dangerous Is Dyspnoea From FERROUS ANHYDROUS?
Of the 106 reports, 13 (12.3%) resulted in death, 105 (99.1%) required hospitalization, and 27 (25.5%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FERROUS ANHYDROUS. However, 106 reports have been filed with the FAERS database.
What Other Side Effects Does FERROUS ANHYDROUS Cause?
Asthma (190)
Full blood count abnormal (160)
Gastrooesophageal reflux disease (151)
Wheezing (103)
Hyperglycaemia (95)
Type 2 diabetes mellitus (95)
Obstructive airways disorder (83)
Sleep disorder due to a general medical condition (81)
Therapeutic product effect incomplete (75)
Foetal exposure during pregnancy (74)
What Other Drugs Cause Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)
Which FERROUS ANHYDROUS Alternatives Have Lower Dyspnoea Risk?
FERROUS ANHYDROUS vs FERROUS GLYCINE
FERROUS ANHYDROUS vs FERROUS\FERROUS, DRIED
FERROUS ANHYDROUS vs FERROUS\FOLIC ACID
FERROUS ANHYDROUS vs FERUMOXYTOL
FERROUS ANHYDROUS vs FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE