The Safety Rates Drug Report

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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
927588010 9275880 10 F 201101 20160818 20130507 20160831 EXP US-JNJFOC-20130416147 JOHNSON AND JOHNSON 38.57 YR A M Y 160.00000 KG 20160831 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
927588010 9275880 1 SS TYLENOL REGULAR STRENGTH ACETAMINOPHEN 1 Oral U U 0 325 MG TABLET
927588010 9275880 2 SS TYLENOL REGULAR STRENGTH ACETAMINOPHEN 1 Oral U U 0 325 MG TABLET
927588010 9275880 3 PS TYLENOL REGULAR STRENGTH ACETAMINOPHEN 1 Oral U U 19872 325 MG TABLET
927588010 9275880 4 SS TYLENOL REGULAR STRENGTH ACETAMINOPHEN 1 Oral U U 19872 325 MG TABLET
927588010 9275880 5 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral 2 PILLS 6 TIMES PER DAY EVERY OTHER DAY FOR THE NEXT 2 WEEKS IMMEDIATELY U U 0 500 MG TABLET
927588010 9275880 6 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral 2 PILLS 6 TIMES PER DAY EVERY OTHER DAY FOR THE NEXT 2 WEEKS IMMEDIATELY U U 0 500 MG TABLET
927588010 9275880 7 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral 2 PILLS 6 TIMES PER DAY EVERY OTHER DAY FOR THE NEXT 2 WEEKS IMMEDIATELY U U 19872 500 MG TABLET
927588010 9275880 8 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral 2 PILLS 6 TIMES PER DAY EVERY OTHER DAY FOR THE NEXT 2 WEEKS IMMEDIATELY U U 19872 500 MG TABLET
927588010 9275880 9 SS TYLENOL ACETAMINOPHEN 1 Oral U U 0 TABLET
927588010 9275880 10 SS TYLENOL ACETAMINOPHEN 1 Oral U U 0 TABLET
927588010 9275880 11 SS TYLENOL ACETAMINOPHEN 1 Oral U U 0 TABLET
927588010 9275880 12 SS TYLENOL ACETAMINOPHEN 1 Oral U U 0 TABLET
927588010 9275880 13 SS TYLENOL ACETAMINOPHEN 1 Oral U U 0 TABLET
927588010 9275880 14 SS TYLENOL ACETAMINOPHEN 1 Oral U U 0 TABLET
927588010 9275880 15 SS TYLENOL ACETAMINOPHEN 1 Oral U U 19872 TABLET
927588010 9275880 16 SS TYLENOL ACETAMINOPHEN 1 Oral U U 19872 TABLET
927588010 9275880 17 SS ALCOHOL. ALCOHOL 1 Oral APPROXIMATELY THREE TO FOUR DRINKS AND AT TIMES ALMOST EVERY OTHER DAY U 0 LIQUID
927588010 9275880 18 SS NSAID UNSPECIFIED INGREDIENT 1 Unknown U 0 UNSPECIFIED
927588010 9275880 19 SS NSAID UNSPECIFIED INGREDIENT 1 Unknown U 0 UNSPECIFIED
927588010 9275880 20 SS ALEVE NAPROXEN SODIUM 1 Oral 4 TO 8 TABLETS PER WEEK, RECENTLY INCREASED UP TO 8-10 TABLETS PER DAY U 0 TABLET
927588010 9275880 21 SS ALEVE NAPROXEN SODIUM 1 Oral 4 TO 8 TABLETS PER WEEK, RECENTLY INCREASED UP TO 8-10 TABLETS PER DAY U 0 TABLET
927588010 9275880 22 SS ORLISTAT ORLISTAT 1 Unknown U 0 UNSPECIFIED
927588010 9275880 23 SS PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown U 0 UNSPECIFIED
927588010 9275880 24 SS PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown U 0 UNSPECIFIED
927588010 9275880 25 SS MUSCLE RELAXANT UNSPECIFIED INGREDIENT 1 Oral ABOUT 2 TABLETS EVERY 6 HOURS U 0 TABLET
927588010 9275880 26 C ALLI ORLISTAT 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
927588010 9275880 1 Arthralgia
927588010 9275880 2 Back pain
927588010 9275880 3 Chills
927588010 9275880 4 Pyrexia
927588010 9275880 5 Arthralgia
927588010 9275880 6 Back pain
927588010 9275880 7 Chills
927588010 9275880 8 Pyrexia
927588010 9275880 9 Arthritis
927588010 9275880 10 Chest pain
927588010 9275880 11 Respiratory tract congestion
927588010 9275880 12 Cough
927588010 9275880 13 Oropharyngeal pain
927588010 9275880 14 Pain
927588010 9275880 15 Headache
927588010 9275880 16 Pyrexia
927588010 9275880 17 Product used for unknown indication
927588010 9275880 18 Arthritis
927588010 9275880 19 Pain management
927588010 9275880 20 Arthritis
927588010 9275880 21 Pain management
927588010 9275880 22 Product used for unknown indication
927588010 9275880 23 Pain management
927588010 9275880 24 Arthritis
927588010 9275880 25 Arthritis
927588010 9275880 26 Weight decreased

Outcome of event

Event ID CASEID OUTC COD
927588010 9275880 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
927588010 9275880 Acute hepatic failure
927588010 9275880 Jaundice
927588010 9275880 Toxicity to various agents

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
927588010 9275880 1 2010 0
927588010 9275880 2 2010 0
927588010 9275880 3 2010 0
927588010 9275880 4 2010 0
927588010 9275880 5 2010 0
927588010 9275880 6 2010 0
927588010 9275880 7 2010 0
927588010 9275880 8 2010 0
927588010 9275880 9 201002 0
927588010 9275880 10 201002 0
927588010 9275880 11 201002 0
927588010 9275880 12 201002 0
927588010 9275880 13 201002 0
927588010 9275880 14 201002 0
927588010 9275880 15 201002 0
927588010 9275880 16 201002 0
927588010 9275880 26 201012 0