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
107290822 10729082 2 F 1999 20150109 20150122 20160831 EXP US-JNJFOC-20150108726 JANSSEN 0.00 F Y 0.00000 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
107290822 10729082 1 PS PEPCID FAMOTIDINE 1 Unknown U U 20325 UNSPECIFIED
107290822 10729082 2 SS PEPCID FAMOTIDINE 1 Unknown U U 20325 UNSPECIFIED
107290822 10729082 3 SS FENTANYL. FENTANYL 1 Unknown U 19813 UNSPECIFIED
107290822 10729082 4 SS LEVAQUIN LEVOFLOXACIN 1 Unknown U U 20634 UNSPECIFIED
107290822 10729082 5 SS MIDRIN ACETAMINOPHENDICHLORALPHENAZONEISOMETHEPTENE 1 Unknown U 0 UNSPECIFIED
107290822 10729082 6 SS METAMUCIL PLANTAGO SEED 1 Unknown U 0 UNSPECIFIED
107290822 10729082 7 SS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown U 0 UNSPECIFIED
107290822 10729082 8 SS DANTROLENE DANTROLENE 1 Unknown ONE CAPSULE U 0 25 MG CAPSULE
107290822 10729082 9 SS ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 Unknown ONE IN THE MORNING AND ONE AT NIGHT U 0 2 MG TABLETS BID
107290822 10729082 10 SS METHADONE METHADONE HYDROCHLORIDE 1 Unknown 2 PILLS U 0 UNSPECIFIED
107290822 10729082 11 SS CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Unknown U 0 UNSPECIFIED
107290822 10729082 12 SS NEURONTIN GABAPENTIN 1 Unknown U 0 UNSPECIFIED
107290822 10729082 13 SS NEURONTIN GABAPENTIN 1 Unknown U 0 100 MG UNSPECIFIED
107290822 10729082 14 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown U 0 UNSPECIFIED
107290822 10729082 15 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown U 0 UNSPECIFIED
107290822 10729082 16 SS UNSPECIFIED ROBITUSSIN GUAIFENESIN 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107290822 10729082 2 Product used for unknown indication
107290822 10729082 3 Product used for unknown indication
107290822 10729082 4 Product used for unknown indication
107290822 10729082 5 Product used for unknown indication
107290822 10729082 6 Product used for unknown indication
107290822 10729082 7 Product used for unknown indication
107290822 10729082 8 Product used for unknown indication
107290822 10729082 9 Product used for unknown indication
107290822 10729082 10 Product used for unknown indication
107290822 10729082 11 Product used for unknown indication
107290822 10729082 12 Product used for unknown indication
107290822 10729082 13 Product used for unknown indication
107290822 10729082 14 Product used for unknown indication
107290822 10729082 15 Product used for unknown indication
107290822 10729082 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
107290822 10729082 OT
107290822 10729082 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
107290822 10729082 Abasia
107290822 10729082 Abdominal pain upper
107290822 10729082 Asthenia
107290822 10729082 Biliary colic
107290822 10729082 Eye swelling
107290822 10729082 Malaise
107290822 10729082 Meningitis aseptic
107290822 10729082 Multiple allergies
107290822 10729082 Oedema
107290822 10729082 Oxygen saturation decreased
107290822 10729082 Pneumonia
107290822 10729082 Pruritus
107290822 10729082 Sedation
107290822 10729082 Vision blurred

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
107290822 10729082 3 201409 0
107290822 10729082 10 201409 0
107290822 10729082 12 199911 0
107290822 10729082 13 1999 0