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
126688261 12668826 1 I 20160302 20160819 20160819 PER US-ASTELLAS-2016US008028 ASTELLAS 51.00 YR F Y 0.00000 20160819 CN GB 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
126688261 12668826 1 PS AMBISOME AMPHOTERICIN B 1 Unknown 50740 4 MG/KG INJECTION
126688261 12668826 2 SS IBUPROFEN. IBUPROFEN 1 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126688261 12668826 3 SS NORMAL SALINE SODIUM CHLORIDE 1 Unknown UNK UNK, CONTINUOUS U 0 FORMULATION UNKNOWN
126688261 12668826 4 SS NORMAL SALINE SODIUM CHLORIDE 1 Unknown UNK UNK, TWICE DAILY 0 FORMULATION UNKNOWN BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126688261 12668826 1 Meningitis cryptococcal
126688261 12668826 2 Product used for unknown indication
126688261 12668826 3 Meningitis cryptococcal

Outcome of event

Event ID CASEID OUTC COD
126688261 12668826 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126688261 12668826 Blood creatinine increased
126688261 12668826 Drug interaction
126688261 12668826 Headache
126688261 12668826 Nephropathy toxic
126688261 12668826 Product preparation error
126688261 12668826 Wrong technique in product usage process

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

no results found

Therapies reported

no results found