AMMONIUM LACTATE
Generic: AMMONIUM LACTATE
Sun Pharmaceutical IndustriesManufacturer
TOPICALRoute
AMMONIUM LACTATEActive Substance
2004-05-28Original Approval
AMMONIUM LACTATE is FDA application ANDA076216, sponsored by SUN PHARMA CANADA. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
FATIGUE
149 reports
2
PAIN
148 reports
3
DIARRHOEA
140 reports
4
DRUG INEFFECTIVE
134 reports
5
CHRONIC KIDNEY DISEASE
127 reports
6
NAUSEA
126 reports
7
DYSPNOEA
115 reports
8
RASH
110 reports
9
FALL
109 reports
10
HEADACHE
104 reports