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
125286414 12528641 4 F 200104 20160826 20160705 20160908 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201606-003270 CONCORDIA 41.00 YR F Y 0.00000 20160908 OT GB GB

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
125286414 12528641 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown UNK U 21959
125286414 12528641 2 SS Tranylcypromine TRANYLCYPROMINE 1 Unknown UNK U 12342
125286414 12528641 3 SS ORAPRED PREDNISOLONE SODIUM PHOSPHATE 1 Unknown UNK 21959
125286414 12528641 4 SS PAROXETINE. PAROXETINE 1 Unknown 30 MG, QD 3748.75 MG U 0 30 MG QD
125286414 12528641 5 SS PAROXETINE. PAROXETINE 1 Unknown 3748.75 MG U 0 20 MG TABLET
125286414 12528641 6 SS PAROXETINE. PAROXETINE 1 Unknown 30 MG, QD 3748.75 MG U 0 30 MG TABLET QD
125286414 12528641 7 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, QD 3748.75 MG U 0 20 MG QD
125286414 12528641 8 SS PAROXETINE. PAROXETINE 1 Unknown 20 MG, QD 3748.75 MG U 0 20 MG TABLET QD
125286414 12528641 9 SS PAROXETINE. PAROXETINE 1 Unknown 30 MG, UNK 3748.75 MG U 0 30 MG
125286414 12528641 10 SS PAROXETINE. PAROXETINE 1 Unknown 30 MG, UNK 3748.75 MG U 0 30 MG
125286414 12528641 11 SS PAROXETINE. PAROXETINE 1 Unknown 3748.75 MG U 0 30 MG TABLET
125286414 12528641 12 SS PAROXETINE. PAROXETINE 1 Unknown 30 MG, QD 3748.75 MG U 0 30 MG TABLET QD
125286414 12528641 13 SS PAROXETINE. PAROXETINE 1 Unknown 3748.75 MG U 0 20 MG QD
125286414 12528641 14 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown 30 MG, U U 0 30 MG TABLET
125286414 12528641 15 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Endocervical 20 MG, U U 0 20 MG
125286414 12528641 16 SS SEROXAT PAROXETINE HYDROCHLORIDE 1 Unknown 20 MG, U 0 20 MG
125286414 12528641 17 SS SEROXAT PAROXETINE HYDROCHLORIDE 1 Unknown 30 MG, U 0 30 MG
125286414 12528641 18 C PROCHLORPERAZINE. PROCHLORPERAZINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125286414 12528641 1 Asthma
125286414 12528641 2 Product used for unknown indication
125286414 12528641 3 Asthma
125286414 12528641 4 Depression
125286414 12528641 5 Depression
125286414 12528641 14 Depression
125286414 12528641 16 Depression
125286414 12528641 18 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125286414 12528641 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125286414 12528641 Anger
125286414 12528641 Anxiety
125286414 12528641 Condition aggravated
125286414 12528641 Dizziness
125286414 12528641 Drug withdrawal syndrome
125286414 12528641 Dyssomnia
125286414 12528641 Feeling cold
125286414 12528641 Headache
125286414 12528641 Hot flush
125286414 12528641 Hyperhidrosis
125286414 12528641 Hypoaesthesia
125286414 12528641 Mood swings
125286414 12528641 Muscle spasms
125286414 12528641 Nausea
125286414 12528641 Obsessive-compulsive disorder
125286414 12528641 Paraesthesia
125286414 12528641 Suicidal ideation
125286414 12528641 Vomiting
125286414 12528641 Weight increased

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
125286414 12528641 5 20001127 20010608 0
125286414 12528641 6 20001127 2001 0
125286414 12528641 7 20001127 20010608 0
125286414 12528641 8 20001127 2001 0
125286414 12528641 10 20010126 20010608 0
125286414 12528641 11 20010126 20010608 0
125286414 12528641 12 20001127 2001 0
125286414 12528641 13 20001127 20010608 0
125286414 12528641 15 20001127 20010608 0
125286414 12528641 16 20001127 20010608 0