92 reports of this reaction
3.0% of all PHOSPHORIC ACID reports
#12 most reported adverse reaction
SEDATION is the #12 most commonly reported adverse reaction for PHOSPHORIC ACID, manufactured by BM Private Limited. There are 92 FDA adverse event reports linking PHOSPHORIC ACID to SEDATION. This represents approximately 3.0% of all 3,032 adverse event reports for this drug.
Patients taking PHOSPHORIC ACID who experience sedation should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SEDATION is a less commonly reported adverse event for PHOSPHORIC ACID, but still significant enough to appear in the safety profile.
In addition to sedation, the following adverse reactions have been reported for PHOSPHORIC ACID:
The following drugs have also been linked to sedation in FDA adverse event reports:
SEDATION has been reported as an adverse event in 92 FDA reports for PHOSPHORIC ACID. This does not prove causation, but indicates an association observed in post-market surveillance data.
SEDATION accounts for approximately 3.0% of all adverse event reports for PHOSPHORIC ACID, making it a notable side effect.
If you experience sedation while taking PHOSPHORIC ACID, 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.