103 reports of this reaction
1.4% of all PENICILLIN V POTASSIUM reports
#17 most reported adverse reaction
FULL BLOOD COUNT ABNORMAL is the #17 most commonly reported adverse reaction for PENICILLIN V POTASSIUM, manufactured by Aurobindo Pharma Limited. There are 103 FDA adverse event reports linking PENICILLIN V POTASSIUM to FULL BLOOD COUNT ABNORMAL. This represents approximately 1.4% of all 7,202 adverse event reports for this drug.
Patients taking PENICILLIN V POTASSIUM who experience full blood count abnormal should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FULL BLOOD COUNT ABNORMAL is a less commonly reported adverse event for PENICILLIN V POTASSIUM, but still significant enough to appear in the safety profile.
In addition to full blood count abnormal, the following adverse reactions have been reported for PENICILLIN V POTASSIUM:
The following drugs have also been linked to full blood count abnormal in FDA adverse event reports:
FULL BLOOD COUNT ABNORMAL has been reported as an adverse event in 103 FDA reports for PENICILLIN V POTASSIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
FULL BLOOD COUNT ABNORMAL accounts for approximately 1.4% of all adverse event reports for PENICILLIN V POTASSIUM, making it a notable side effect.
If you experience full blood count abnormal while taking PENICILLIN V POTASSIUM, 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.