Copper Topical Side Effects
Applies to copper topical: intrauterine device.
Genitourinary adverse events
Genitourinary side effects including intrauterine pregnancy, septic abortion, ectopic pregnancy, pelvic infection, perforation, embedment, pregnancy, bleeding/pain, other medical events, dysmenorrhea, dyspareunia, complete or partial expulsion, leukorrhea, prolonged menstrual flow, menstrual spotting, pain and cramping, and vaginitis have been reported.[Ref]
Hematologic
Hematologic side effects including anemia have been reported.[Ref]
Musculoskeletal
Musculoskeletal side effects including backache have been reported.[Ref]
Dermatologic
Dermatologic side effects including urticarial allergic skin reaction have been reported.[Ref]
See also:
Mirena
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Provera
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Botox
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Depo Provera
Depo-Provera is used as contraception to prevent pregnancy. It is also used to reduce pain cause by ...
Nexplanon
Nexplanon is a long-term, reversible birth control implant that lasts for three years. Learn about ...
Sprintec
Sprintec is used for abnormal uterine bleeding, birth control, endometriosis, gonadotropin ...
Yaz
Yaz (drospirenone and ethinyl estradiol) is used as a contraceptive to prevent pregnancy. Includes ...
Slynd
Slynd (drospirenone) is a birth control pill used for the prevention of pregnancy. Includes Slynd ...
Lo Loestrin Fe
Lo Loestrin Fe (ethinyl estradiol and norethindrone acetate) birth control tablets are used to ...
Medroxyprogesterone
Medroxyprogesterone (Provera) treats conditions such as absent or irregular menstrual periods, or ...
References
1. (2009) "Product Information. ParaGard (copper)." Barr Pharmaceuticals Inc
More about copper topical
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- Drug class: miscellaneous vaginal agents
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Further information
Copper topical side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.
