Safety Rates Drug Report: adverse events in 2016 Q3 - FDA prescription drugs adverse events in an open, searchable, online, public database

Drug Injury Quarter

Person who experienced the adverse event (patient)

Event ID	CASEID	CASEVERSION	I F COD	EVENT DT	MFR DT	INIT FDA DT	FDA DT	REPT COD	AUTH NUM	MFR NUM	MFR SNDR	LIT REF	AGE	AGE COD	AGE GRP	GNDR COD	E SUB	WT	WT COD	REPT DT	TO MFR	OCCP COD	REPORTER COUNTRY	OCCR COUNTRY
126228002	12622800	2	F		20160829	20160804	20160906	EXP		DK-JNJFOC-20160724285	JANSSEN		50.00	YR	A	F	Y	0.00000		20160906		MD	DK	DK

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DECHAL	RECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126228002	12622800	1	PS	DARUNAVIR	DARUNAVIR	1	Oral	U	U	21976	600	MG	TABLETS	BID
126228002	12622800	2	SS	RETROVIR	ZIDOVUDINE	1	Unknown	U		0			UNSPECIFIED
126228002	12622800	3	SS	MARAVIROC	MARAVIROC	1	Unknown	U		0	150	MG	TABLET	BID
126228002	12622800	4	SS	NORVIR	RITONAVIR	1	Unknown	U		0	100	MG	UNSPECIFIED	BID
126228002	12622800	5	SS	COMBIVIR	LAMIVUDINEIDOVUDINE	1	Unknown	U		0	1	DF	TABLET	BID
126228002	12622800	6	SS	DOLUTEGRAVIR	DOLUTEGRAVIR	1	Unknown	U		0			UNSPECIFIED

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126228002	12622800	1	Acquired immunodeficiency syndrome
126228002	12622800	2	Acquired immunodeficiency syndrome
126228002	12622800	3	Acquired immunodeficiency syndrome
126228002	12622800	4	Acquired immunodeficiency syndrome
126228002	12622800	5	Acquired immunodeficiency syndrome
126228002	12622800	6	Acquired immunodeficiency syndrome

Outcome of event

Event ID	CASEID	OUTC COD
126228002	12622800	OT

Reactions reported

Event ID	CASEID	PT
126228002	12622800	Anaemia
126228002	12622800	Pathogen resistance
126228002	12622800	Treatment noncompliance
126228002	12622800	Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

no results found

Therapies reported

no results found

no results found