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
1037359813 10373598 13 F 20080614 20160915 20140808 20160928 EXP US-JNJFOC-20140803225 JOHNSON AND JOHNSON 45.34 YR A F Y 70.31000 KG 20160928 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
1037359813 10373598 1 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral Y N 0 6 DF TABLETS
1037359813 10373598 2 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral EVERY 4-6 HOURS, SEVERAL TIMES A WEEK, MAXIMUM OF 6-8 PILLS Y N 0 650 MG TABLETS
1037359813 10373598 3 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral EVERY 4-6 HOURS, SEVERAL TIMES A WEEK, MAXIMUM OF 6-8 PILLS Y N 0 650 MG TABLETS
1037359813 10373598 4 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral Y N 0 6 DF TABLETS
1037359813 10373598 5 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral Y N 0 6 DF TABLETS
1037359813 10373598 6 PS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral EVERY 4-6 HOURS, SEVERAL TIMES A WEEK, MAXIMUM OF 6-8 PILLS Y N 999999 650 MG TABLETS
1037359813 10373598 7 SS TYLENOL PM ACETAMINOPHENDIPHENHYDRAMINE 1 Unknown 5 TO 7 WITH 500 MG OF TYLENOL IN EACH PILL U U UNKNOWN 999999 UNSPECIFIED
1037359813 10373598 8 C VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown 2 OVER THE PAST WEEK D 0 UNSPECIFIED
1037359813 10373598 9 C LYRICA PREGABALIN 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 10 C XANAX ALPRAZOLAM 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 11 C IMITREX SUMATRIPTAN SUCCINATE 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 12 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) AS NECCESSARY D 0 UNSPECIFIED
1037359813 10373598 13 C BABY ASPIRIN ASPIRIN 1 Oral D 0 CHEWABLE TABLET
1037359813 10373598 14 C NITROSPRAY 2 Sublingual D 0 SPRAY
1037359813 10373598 15 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 16 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 17 C IBUPROFEN. IBUPROFEN 1 Unknown D 0 800 MG UNSPECIFIED TID
1037359813 10373598 18 C NAPROXEN. NAPROXEN 1 Unknown D 0 375 MG TABLET TID
1037359813 10373598 19 C NAPROXEN. NAPROXEN 1 Unknown D 0 375 MG TABLET TID
1037359813 10373598 20 C SOMA CARISOPRODOL 1 Unknown D 0 350 MG TABLET Q6H
1037359813 10373598 21 C TORADOL KETOROLAC TROMETHAMINE 1 Intramuscular D 0 60 MG INJECTION
1037359813 10373598 22 C MOTRIN IBUPROFEN 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 23 C MOTRIN IBUPROFEN 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 24 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 25 C DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Unknown D 0 UNSPECIFIED
1037359813 10373598 26 C PROTONIX PANTOPRAZOLE SODIUM 1 Unknown D 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1037359813 10373598 1 Pain
1037359813 10373598 2 Pain
1037359813 10373598 3 Headache
1037359813 10373598 4 Headache
1037359813 10373598 5 Fibromyalgia
1037359813 10373598 6 Fibromyalgia
1037359813 10373598 7 Product used for unknown indication
1037359813 10373598 8 Fibromyalgia
1037359813 10373598 9 Fibromyalgia
1037359813 10373598 10 Anxiety
1037359813 10373598 11 Migraine
1037359813 10373598 12 Asthma
1037359813 10373598 13 Product used for unknown indication
1037359813 10373598 14 Product used for unknown indication
1037359813 10373598 15 Product used for unknown indication
1037359813 10373598 16 Product used for unknown indication
1037359813 10373598 17 Product used for unknown indication
1037359813 10373598 18 Inflammation
1037359813 10373598 19 Pain
1037359813 10373598 20 Product used for unknown indication
1037359813 10373598 21 Product used for unknown indication
1037359813 10373598 22 Arthralgia
1037359813 10373598 23 Pain in extremity
1037359813 10373598 24 Product used for unknown indication
1037359813 10373598 25 Product used for unknown indication
1037359813 10373598 26 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1037359813 10373598 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
1037359813 10373598 Acute hepatic failure
1037359813 10373598 Acute kidney injury
1037359813 10373598 Brain oedema
1037359813 10373598 Drug ineffective for unapproved indication
1037359813 10373598 Intentional overdose
1037359813 10373598 Lactic acidosis
1037359813 10373598 Metabolic acidosis
1037359813 10373598 Product use issue
1037359813 10373598 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
1037359813 10373598 2 1990 200806 0
1037359813 10373598 3 1990 200806 0
1037359813 10373598 6 1990 200806 0
1037359813 10373598 8 2006 2008 0
1037359813 10373598 10 2008 0
1037359813 10373598 13 20080612 0
1037359813 10373598 14 20080612 0
1037359813 10373598 17 200701 0
1037359813 10373598 18 200701 0
1037359813 10373598 19 200701 0
1037359813 10373598 20 200701 0
1037359813 10373598 21 20070110 0
1037359813 10373598 22 200801 0
1037359813 10373598 23 200801 0
1037359813 10373598 24 200801 0
1037359813 10373598 25 200801 0