AMMONIA N 13
Generic: AMMONIA N-13
PETNET SolutionsManufacturer
INTRAVENOUSRoute
AMMONIA N-13Active Substance
2015-11-02Original Approval
AMMONIA N 13 is FDA application ANDA204510, sponsored by PETNET. 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
DRUG ABUSE
7 reports
2
COUGH
6 reports
3
DEPRESSION
6 reports
4
DRUG INEFFECTIVE
6 reports
5
CHEST PAIN
5 reports
6
DYSPNOEA
5 reports
7
NAUSEA
5 reports
8
SUICIDE ATTEMPT
5 reports
9
VOMITING
5 reports
10
ACCIDENTAL EXPOSURE TO PRODUCT
4 reports