how to fill adr reporting form and causality assessmentwebsite.aiimsraipur.edu.in/downloads/how to...
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![Page 1: How to fill ADR Reporting Form and Causality Assessmentwebsite.aiimsraipur.edu.in/Downloads/How to fill... · Co-coordinator , ADR Monitoring Center, PvPI Associate Professor, Pharmacology](https://reader034.vdocument.in/reader034/viewer/2022042909/5f3ba902dd500f1cd753a88f/html5/thumbnails/1.jpg)
Dr. Nitin GaikwadCo-coordinator , ADR Monitoring Center, PvPI
Associate Professor, PharmacologyAIIMS Raipur
How to fill ADR Reporting Form andCausality Assessment
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• Suspected Adverse Drug Reaction Reporting Form(For voluntary reporting of Adverse Drug Reactions by Healthcare Professionals)
• ADR Reporting Form for Consumer
• Transfusion Reaction Reporting Form (TRRF)(Haemovigilance Program of India)
• Medical Device Adverse Event Reporting Form(Materiovigilance Program of India)
ADR Reporting Forms
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Who can report?
Doctor Dentist
PharmacistNurse
Patient
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• Nearest ADR Monitoring Center (AMC)– AIIMS Raipur– Pt. JNMC, Raipur
• Directly to NCC, IPC Ghaziabad
• [email protected]@ipcindia.net
• Toll free no. – 1800 180 3024
• ADR Reporting Android app
Where to report
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• Serious or Non-serious ADR
• Known or Unknown ADR
• Frequent or Rare
– Related to medicine, vaccine, herbal products
What to report?
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A. Patient Information
1 Patient Initials
2 Age at the time of Event or Date of Birth
3SexMale Female Other
4 Weight (kg)
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B. Suspected Adverse Reaction
5 Date of Reaction started (dd/mm/yyyy)
6 Date of recovery (dd/mm/yyyy)
7 Describe reaction or problem
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C. Suspected Medication8 Name (Brand and/or Generic)
Manufacturer (if known)
Batch No. /Lot No.
Exp. Date (if known)
Dose used
Route used
Frequency (OD, BD, etc)
Therapy datesDate Started Date Stopped
Indication
Causality Assessment
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C. Suspected Medication
9Action Taken (Please tick)Drug Withdrawn
Doseincreased
Dose reduced
Dose not changed
Notapplicable
Unknown
i
ii
iii
iv
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C. Suspected Medication
10
Reaction reappeared after reintroduction (please tick)
Yes No Effect unknownDose (if
reintroduced)
i
ii
iii
iv
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C. Suspected Medication
11
Concomitant medical products Including self-medication and herbal remedies with therapy dates (Exclude those used to treat reaction)
Name(Brand/
Generic)
Dose used
Route Used
Frequency(OD, BD,
etc.)
Therapy dates
IndicationDate Started
Date Stopped
i
ii
iii
iv
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12 Relevant tests/laboratory data with dates
13Relevant medical / medication history(e.g. allergies, race, pregnancy, smoking, alcohol use, hepatic/renal dysfunction etc.)
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14Seriousness of the reaction: No If Yes (Please tick anyone)
Death (dd/mm/yyyy)
Life threatening
Hospitalization (initial or prolonged)
Disability
Congenital anomaly
Required intervention to prevent permanent impairment / damage
Other (specify)
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15 Outcomes
Recovered
Recovering
Not recovered
Fatal
Recovered with sequelae
Unknown
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D. Reporter Details
16
Name and Professional Address
Pin Email
Tel. No. (with STD Code)
Occupation Signature
17 Date of this report (dd/mm/yyyy)
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Mandatory Fields for Suspected ADR Reporting Form
Patient initials
Age at onset of reaction
Date of onset of reaction
Reaction term(s)
Suspected medication
Reporter information
1
2
5
7
8
16, 17
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• Vigiflow software
Safety Database
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• Vigiflow software
Safety Database
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ADR Case – 1
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Madan Lal, a 65-years old male patient admitted to hospital on 12.01.2016 with chiefcomplaints of pain in upper abdomen and nausea since last 5 days. On physicalexamination, he had yellowish discoloration of palm, conjunctiva and nail bed. Hisweight was 72 kg.
He had few episodes of psychotic attacks, for which he was on Chlorpromazinetherapy since last 4 weeks. On enquiry, he told that he was taking Tab. Largactil(Chlorpromazine) 100 mg, 4 tablets at bed time.
He was also taking Tab. Diclofenac 50 mg twice-a-day (self-medication) forabdominal pain for three days before admitting to hospital. He was investigated onthe day of admission for laboratory parameters which are as follows:
– Alkaline Phosphatase = 180 U/L (Normal range: 25 – 100 U/L)
– ALT = 205 U/L (Normal range: 10 – 40 Units/L)
– Total Bilirubin = 5.0 mg/dL (Normal range: 0.8 – 1.2 mg/dL)
On admission, Chlorpromazine and Diclofenac therapy was stopped. After 7 days ofstopping the medications, the intensity of pain decreased. Also, he was reinvestigated for above parameters which are as follows:
– Alkaline Phosphatase = 110 IU/L
– ALT = 98 Units/L
– Total Bilirubin = 1.8 mg/dL
• Note: Tab ChlorpromazineBrand Name: LARGACTIL, Manufacturer: Wedley labsBatch number: LGL0881, Expiry date: Dec 2018
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A. Patient Information
1 Patient Initials – ML
2 Age at the time of Event or Date of Birth – 65 years
3SexMale Female Other
4 Weight (kg) – 72 kg
3
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B. Suspected Adverse Reaction
5 Date of Reaction started (dd/mm/yyyy): 07.01.2016
6 Date of recovery (dd/mm/yyyy):
7
Describe reaction or problemPatient was taking Chlorpromazine since 12.12.2015. He developed painin abdomen and nausea since 07.01.2016. Examination revealed yellowishdiscoloration of conjunctiva, palm and nails. Pt. was admitted on12.01.2016 and investigated. Liver function tests indicated raised serumbilirubin, ALT and alkaline phosphatase. Drugs were discontinued. Ondiscontinuation of drug, reaction subsided in one week.
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C. Suspected Medication8 Name (Brand and/or Generic): Tab. Chlorpromazine (Largactil)
Manufacturer (if known): Wedley labs
Batch No. /Lot No.: LGL0881
Exp. Date (if known): Dec. 2018
Dose used: 400 mg
Route used: Oral
Frequency (OD, BD, etc): OD
Therapy datesDate Started 12.12.2015 Date Stopped 12.01.2016
Indication: Psychosis
Causality Assessment: Probable
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C. Suspected Medication
9Action Taken (Please tick)Drug Withdrawn
Doseincreased
Dose reduced
Dose not changed
Notapplicable
Unknown
i f
ii
iii
iv
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C. Suspected Medication
10
Reaction reappeared after reintroduction (please tick)
Yes NoEffect
unknownDose (if
reintroduced)
i
ii
iii
iv
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C. Suspected Medication
11
Concomitant medical products Including self-medication and herbal remedies with therapy dates (Exclude those used to treat reaction)
Name(Brand/
Generic)
Dose used
Route Used
Frequency(OD, BD,
etc.)
Therapy dates
IndicationDate Started
Date Stopped
iTab.
Diclofenac50 mg Oral BD
09.01.2016
12.01.2016
Pain in abdomen
ii
iii
iv
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12
Relevant tests/laboratory data with dates12.01.2016 19.01.2016Alkaline Phosphatase = 180 U/L Alkaline Phosphatase = 110 U/LALT = 205 U/L ALT = 98 U/LTotal Bilirubin = 5.0 mg/dL Total Bilirubin = 1.8 mg/dL
13Relevant medical / medication history(e.g. allergies, race, pregnancy, smoking, alcohol use, hepatic/renal dysfunction etc.)
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14Seriousness of the reaction: No If Yes (Please tick anyone)
Death (dd/mm/yyyy)
Life threatening
fHospitalization (Initial or prolonged)
Disability
Congenital anomaly
Required intervention to prevent permanent impairment / damage
Other (specify)
h
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15 Outcomes
Recovered
g Recovering
Not recovered
Fatal
Recovered with sequelae
Unknown
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D. Reporter Details
16
Name and Professional Address: Dr. A. K. Jain, Dept. of Medicine, AIIMS Raipur
Pin 492099 Email [email protected]
Tel. No. (with STD Code): 0771-2563452
Occupation Doctor Signature
17 Date of this report (dd/mm/yyyy): 23.01.2016
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Causality Assessment – ADR Case 1
CategoriesTime
sequence
Other drugdisease
ruled outDechallenge Rechallenge
Certain Yes Yes Yes Yes
Probable Yes Yes Yes No
Possible Yes No No No
Unlikely No No No No
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ADR Case – 2
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Mr Sushant A Gupta, a 30-years old male with 68 kg weight was diagnosed as a caseof bacterial meningitis. He was started empirically with Inj Ceftriaxone 1 g IV BD andInj Vancomycin 500 mg IV QID on 12.01.2016. First dose of Inj. Ceftriaxone was givenat 8 am and Inj. Vancomycin was given at 9 am on 12.01.2016. After 10 minutes ofsecond drug administration, he started developing chills, rigors, fever, urticaria andintense flushing. He was treated with Inj. Pheniramine 25 mg IM, following which thereaction completely subsided. Inj. Ceftriaxone was continued. However, next doses ofInj. Vancomycin scheduled on day 1 were not given. On day 2, the Inj Vancomycinwas re-introduced at 9 am to the patient. Similar symptoms developed again andquickly resolved after Inj. Pheniramine 25 mg IM.
Note: • Inj Vancomycin
– Brand Name: Vanzid– Manufacturer: SWACH Healthcare– Batch number: KKIL098– Expiry date: Mar 2016
• Inj Ceftriaxone– Brand Name: Taximax– Manufacturer: Wedley Labs– Batch number: OPO659– Expiry date: Dec 2016
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Causality Assessment – ADR Case 1
CategoriesTime
sequence
Other drugdisease
ruled outDechallenge Rechallenge
Certain Yes Yes Yes Yes
Probable Yes Yes Yes No
Possible Yes No No No
Unlikely No No No No
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Thank you…!