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
110892218 11089221 8 F 201304 20160805 20150505 20160820 EXP US-JNJFOC-20150424515 JOHNSON AND JOHNSON 27.23 YR A F Y 62.60000 KG 20160820 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
110892218 11089221 1 PS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral N 19872 500 MG TABLET
110892218 11089221 2 SS TYLENOL ACETAMINOPHEN 1 Unknown APPROXIMATELY 8 TO 10 TABLETS PER DAY (ALSO REPORTED AS 6-10 TABLETS PER DAY) N 19872 TABLET
110892218 11089221 3 SS TYLENOL ACETAMINOPHEN 1 Unknown APPROXIMATELY 8 TO 10 TABLETS PER DAY (ALSO REPORTED AS 6-10 TABLETS PER DAY) N 19872 TABLET
110892218 11089221 4 SS TYLENOL ACETAMINOPHEN 1 Oral N 19872 325 MG TABLET
110892218 11089221 5 SS ALKA-SELTZER ANHYDROUS CITRIC ACIDASPIRINSODIUM BICARBONATE 1 Unknown 0 UNSPECIFIED
110892218 11089221 6 SS ALEVE NAPROXEN SODIUM 1 Unknown 0 UNSPECIFIED
110892218 11089221 7 SS ALEVE NAPROXEN SODIUM 1 Unknown 0 UNSPECIFIED
110892218 11089221 8 SS LORTAB ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown 0 UNSPECIFIED
110892218 11089221 9 SS ALL OTHER THERAPEUTICS UNSPECIFIED INGREDIENT 1 Unknown 0 UNSPECIFIED
110892218 11089221 10 SS ALL OTHER THERAPEUTICS UNSPECIFIED INGREDIENT 1 Unknown 0 UNSPECIFIED
110892218 11089221 11 C DOXYCYCLINE HYCLATE. DOXYCYCLINE HYCLATE 1 Unknown 0 TABLET
110892218 11089221 12 C VITAMIN D CHOLECALCIFEROL 1 Unknown 0 TABLET
110892218 11089221 13 C MEDROXYPROGESTERONE ACETATE. MEDROXYPROGESTERONE ACETATE 1 Intramuscular 0 150 MG SUSPENSION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110892218 11089221 1 Abdominal pain
110892218 11089221 2 Sleep disorder therapy
110892218 11089221 3 Pain
110892218 11089221 4 Product used for unknown indication
110892218 11089221 5 Pain
110892218 11089221 6 Sleep disorder therapy
110892218 11089221 7 Pain
110892218 11089221 8 Product used for unknown indication
110892218 11089221 9 Sleep disorder therapy
110892218 11089221 10 Pain
110892218 11089221 11 Product used for unknown indication
110892218 11089221 12 Product used for unknown indication
110892218 11089221 13 Contraception

Outcome of event

Event ID CASEID OUTC COD
110892218 11089221 HO
110892218 11089221 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
110892218 11089221 Accidental overdose
110892218 11089221 Acute hepatic failure
110892218 11089221 Acute kidney injury
110892218 11089221 Autoimmune hepatitis
110892218 11089221 Coagulopathy
110892218 11089221 Drug administration error
110892218 11089221 Hepatic encephalopathy
110892218 11089221 Leukocytosis
110892218 11089221 Metabolic acidosis
110892218 11089221 Respiratory failure
110892218 11089221 Septic shock
110892218 11089221 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
110892218 11089221 1 201304 20130517 0
110892218 11089221 2 2013 0
110892218 11089221 3 2013 0
110892218 11089221 4 2013 0
110892218 11089221 5 2013 0
110892218 11089221 6 201304 0
110892218 11089221 7 201304 0
110892218 11089221 8 201305 0
110892218 11089221 9 2013 0
110892218 11089221 10 2013 0
110892218 11089221 11 2013 0
110892218 11089221 12 2013 0