91 reports of this reaction
3.0% of all PHOSPHORIC ACID reports
#13 most reported adverse reaction
SEDATION COMPLICATION is the #13 most commonly reported adverse reaction for PHOSPHORIC ACID, manufactured by BM Private Limited. There are 91 FDA adverse event reports linking PHOSPHORIC ACID to SEDATION COMPLICATION. This represents approximately 3.0% of all 3,032 adverse event reports for this drug.
Patients taking PHOSPHORIC ACID who experience sedation complication 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 COMPLICATION is a less commonly reported adverse event for PHOSPHORIC ACID, but still significant enough to appear in the safety profile.
In addition to sedation complication, the following adverse reactions have been reported for PHOSPHORIC ACID:
The following drugs have also been linked to sedation complication in FDA adverse event reports:
SEDATION COMPLICATION has been reported as an adverse event in 91 FDA reports for PHOSPHORIC ACID. This does not prove causation, but indicates an association observed in post-market surveillance data.
SEDATION COMPLICATION accounts for approximately 3.0% of all adverse event reports for PHOSPHORIC ACID, making it a notable side effect.
If you experience sedation complication 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.