The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6817976 7875565 I 6817976-5 20100426 20100706 EXP US-JNJCH-2010015408 JNJCH 53 YR M Y 90.7 KG 20100706 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6817976 1014039947 PS ROLAIDS TAB 1 ORAL TEXT:UNSPECIFIED AS NEEDED FLA149
6817976 1014039948 SS EXTRA STRENGTH TYLENOL 1 ORAL TEXT:^A LOT^ GELCAPS UNSPECIFIED
6817976 1014039949 SS EXTRA STRENGTH TYLENOL PM 2 ORAL TEXT:^A LOT^, ^EVERY NIGHT FOR A YEAR^
6817976 1014039950 C DRUG, UNSPECIFIED 2 UNKNOWN TEXT:UNSPECIFIED
6817976 1014039951 C FISH OIL 2 UNKNOWN TEXT:UNSPECIFIED

Indications of drugs used

Event ID DRUG SEQ INDI PT
6817976 1014039947 DYSPEPSIA
6817976 1014039948 HEADACHE
6817976 1014039949 PRODUCT USED FOR UNKNOWN INDICATION
6817976 1014039950 NAUSEA
6817976 1014039951 BLOOD CHOLESTEROL

Outcome of event

Event ID OUTC COD
6817976 OT

Reactions reported

Event ID PT
6817976 DIARRHOEA
6817976 NAUSEA
6817976 PRODUCT QUALITY ISSUE
6817976 VOMITING
6817976 WEIGHT DECREASED

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

no results found

Therapies reported

no results found