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
126861821	12686182	1	I	20160102	20160104	20160825	20160825	PER		US-PERRIGO-16US000071	PERRIGO		49.97	YR		F	Y	118.37000	KG	20160825		CN	US	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM
126861821	12686182	1	PS	NICOTINE POLACRILEX	NICOTINE	1	Buccal	4 MG, SINGLE	Y	4ME1166	90711	4	MG	LOZENGE
126861821	12686182	2	C	OMEPRAZOLE.	OMEPRAZOLE	1	Unknown	40 MG	U	UNKNOWN	0
126861821	12686182	3	C	HYDROCHLOROTHIAZIDE.	HYDROCHLOROTHIAZIDE	1	Unknown	25 MG	U	UNKNOWN	0
126861821	12686182	4	C	FISH OIL	FISH OIL	1	Unknown	UNK	U	UNKNOWN	0
126861821	12686182	5	C	NIACIN.	NIACIN	1	Unknown	UNK	U	UNKNOWN	0
126861821	12686182	6	C	MAGNESIUM	MAGNESIUM	1	Unknown	UNK	U	UNKNOWN	0
126861821	12686182	7	C	MULTIVITAMINS, PLAIN	VITAMINS	1	Unknown	UNK	U	UNKNOWN	0
126861821	12686182	8	C	GLUCOSAMINE MSM		2	Unknown	UNK	U	UNKNOWN	0
126861821	12686182	9	C	ACIDOPHILUS PROBIOTIC		2	Unknown	UNK	U	UNKNOWN	0
126861821	12686182	10	C	LORATADINE.	LORATADINE	1	Unknown	10 MG	U	UNKNOWN	0
126861821	12686182	11	C	VITAMIN D /00107901/	ERGOCALCIFEROL	1	Unknown	UNK	U	UNKNOWN	0

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126861821	12686182	1	Smoking cessation therapy
126861821	12686182	2	Gastrooesophageal reflux disease
126861821	12686182	3	Oedema
126861821	12686182	4	Supplementation therapy
126861821	12686182	5	Supplementation therapy
126861821	12686182	6	Supplementation therapy
126861821	12686182	7	Supplementation therapy
126861821	12686182	8	Arthritis
126861821	12686182	9	Supplementation therapy
126861821	12686182	10	Supplementation therapy
126861821	12686182	11	Supplementation therapy

Outcome of event

no results found

no results found

Reactions reported

Event ID	CASEID	PT
126861821	12686182	Oral discomfort
126861821	12686182	Salivary hypersecretion
126861821	12686182	Throat tightness

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

no results found

no results found

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
126861821	12686182	1	20160102	20160102	0