511 reports of this reaction
3.2% of all AMPICILLIN SODIUM reports
#5 most reported adverse reaction
PREMATURE BABY is the #5 most commonly reported adverse reaction for AMPICILLIN SODIUM, manufactured by Armas Pharmaceuticals Inc.. There are 511 FDA adverse event reports linking AMPICILLIN SODIUM to PREMATURE BABY. This represents approximately 3.2% of all 15,856 adverse event reports for this drug.
Patients taking AMPICILLIN SODIUM who experience premature baby should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PREMATURE BABY is moderately reported among AMPICILLIN SODIUM users, representing a notable but not dominant share of adverse events.
In addition to premature baby, the following adverse reactions have been reported for AMPICILLIN SODIUM:
The following drugs have also been linked to premature baby in FDA adverse event reports:
PREMATURE BABY has been reported as an adverse event in 511 FDA reports for AMPICILLIN SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
PREMATURE BABY accounts for approximately 3.2% of all adverse event reports for AMPICILLIN SODIUM, making it a notable side effect.
If you experience premature baby while taking AMPICILLIN SODIUM, 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.