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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

FERROUS ANHYDROUS for Supplementation therapy: Side Effects & Safety Data

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There are 30 adverse event reports in the FDA FAERS database where FERROUS ANHYDROUS was used for Supplementation therapy.

Most Reported Side Effects for FERROUS ANHYDROUS

Side Effect Reports % Deaths Hosp.
Asthma 190 38.5% 13 95
Full blood count abnormal 160 32.4% 13 79
Gastrooesophageal reflux disease 151 30.6% 0 56
Dyspnoea 106 21.5% 13 105
Wheezing 103 20.9% 11 102
Hyperglycaemia 95 19.2% 0 0
Type 2 diabetes mellitus 95 19.2% 0 0
Obstructive airways disorder 83 16.8% 13 83
Sleep disorder due to a general medical condition 81 16.4% 12 81
Therapeutic product effect incomplete 75 15.2% 11 75
Foetal exposure during pregnancy 74 15.0% 6 19
Condition aggravated 70 14.2% 13 70
Rhinorrhoea 69 14.0% 0 69
Chronic obstructive pulmonary disease 66 13.4% 0 66
Secretion discharge 65 13.2% 0 65

Other Indications for FERROUS ANHYDROUS

Product used for unknown indication (377) Anaemia (28) Hiv infection (17) Foetal exposure during pregnancy (16) Maternal exposure timing unspecified (10)

Other Drugs Used for Supplementation therapy

FOLIC ACID (191) CALCIUM (150) CHOLECALCIFEROL (86) TESTOSTERONE (83) CYANOCOBALAMIN (75) IRON (75) POTASSIUM (73) MAGNESIUM (67) FOLATE (60) ALBUMIN HUMAN (52)

Related Pages

FERROUS ANHYDROUS Full Profile All Supplementation therapy Drugs FERROUS ANHYDROUS Demographics FERROUS ANHYDROUS Timeline