5 reports of this reaction
1.5% of all NICKEL reports
#10 most reported adverse reaction
COVID 19 is the #10 most commonly reported adverse reaction for NICKEL, manufactured by Boiron. There are 5 FDA adverse event reports linking NICKEL to COVID 19. This represents approximately 1.5% of all 344 adverse event reports for this drug.
Patients taking NICKEL who experience covid 19 should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
COVID 19 is a less commonly reported adverse event for NICKEL, but still significant enough to appear in the safety profile.
In addition to covid 19, the following adverse reactions have been reported for NICKEL:
The following drugs have also been linked to covid 19 in FDA adverse event reports:
COVID 19 has been reported as an adverse event in 5 FDA reports for NICKEL. This does not prove causation, but indicates an association observed in post-market surveillance data.
COVID 19 accounts for approximately 1.5% of all adverse event reports for NICKEL, making it a notable side effect.
If you experience covid 19 while taking NICKEL, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.