BETANIS Adverse Event: Hepatic function abnormal

Name: BETANIS Adverse Event: Hepatic function abnormal
Creator: FDATracker

BETANIS Adverse Event: Hepatic function abnormal is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: BETANIS; Product category: Drug; Primary reaction: Hepatic function abnormal.

Primary drug	BETANIS
Product category	Drug
Primary reaction	Hepatic function abnormal
All reactions	Hepatic function abnormal
Seriousness	Serious
Patient outcome	Unknown
Patient sex	Male
All drugs reported	BETANIS; LOXOPROFEN /00890702/; BAKTAR; ROZEREM
Reporter country	JP
Reporter type	2
Report date	20140313
Report ID	10006189

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