Report Adverse Drug Event — Vetnician

Section A — Medicine Information

Search for the suspected medicine from our database. Details will be auto-filled. If not found, enter manually.

Find Medicine

Medicine Name *

Medicine not found? Enter name manually below and leave the search blank.

Manual Medicine Name (if not found above)

Manufacturer (if known)

Product Details

Batch / Lot Number

Very important for batch-related signal detection

Expiry Date

Usage Details

Dose Given

Route of Administration

Frequency

Duration of Use

Date First Given

Date Last Given

Reason for Use / Diagnosis

Section B — Adverse Event Details

Describe what happened. Be as detailed as possible — even partial information is valuable.

Event Timeline

Date of Adverse Event *

Onset Hours After Dose

How many hours after giving the medicine did the reaction start?

Symptoms / Signs Observed *

Vomiting

Diarrhea

Lethargy

Loss of appetite

Itching / Scratching

Skin rash / Hives

Seizure / Convulsion

Trembling / Shaking

Difficulty breathing

Swelling of face

Excessive drooling

Bleeding

Collapse / Unconscious

Hair loss

Muscle weakness

Eye discharge

Increased urination

Lack of effectiveness

Severity *

😟

Mild

Minor discomfort, no treatment needed

😰

Moderate

Vet visit needed, recoverable

🚨

Severe

Hospitalisation or life-threatening

💔

Fatal

Animal did not survive

Outcome

Current Outcome

Days to Recovery (if recovered)

Did event abate after stopping medicine?

Yes No Not stopped Unknown

Did event reappear after reintroduction?

Yes No Not reintroduced Unknown

Treatment Given for Adverse Event

Detailed Description *

Describe what happened in detail

Minimum 30 words recommended for a complete report

Section C — Animal Information

Details about the animal that experienced the adverse event.

Animal Details

Species *

Breed

Age

Weight (kg)

Gender

Overall Health Before Event

Number of Animals Treated

Number of Animals Affected

Breed-Specific Risk Factors

MDR1 Gene Status (Collie, Shepherd breeds)

Positive (MDR1 mutation) Negative (normal) Unknown

Relevant for ivermectin, milbemycin, loperamide and other P-glycoprotein substrates

Concurrent Medicines & Conditions

Other Medicines Being Given at Same Time

Pre-existing Health Conditions

Section D — Supporting Documents

Upload any supporting documents. These significantly strengthen your report and help with causality assessment.

Upload Files

Accepted: PDF, JPG, PNG, DOC, DOCX — Prescriptions, lab reports, vet notes, product photos, photos of the animal

Click to upload documents

Prescriptions · Lab reports · Vet notes · Medicine photos · Animal photos

Max 5 files · 5MB each

Veterinarian's Assessment (if reporting as vet)

Level of Suspicion that Medicine Caused the Event

High Medium Low Unknown

WHO-UMC Causality Assessment

CertainDefinitive causal link

ProbableLikely causal link

PossibleMay be related

UnlikelyDoubtful causal link

ConditionalMore data needed

UnassessableCannot be assessed

WHO-UMC causality scale — used by CDSCO and global pharmacovigilance databases

Section E — Reporter Information

Your information is held in strict confidence and protected under Indian law. It will not be shared publicly.

Who Are You?

Pet Owner Veterinarian Pharmacist Researcher

Your Contact Details

Your Name

Email Address

Phone Number

City

State

PIN Code

Veterinarian Details

Veterinarian Name

VCI License Number

Pet Owner Details (if different from reporter)

Owner Name

Owner Phone

Confidentiality: Your identity is held in strict confidence and protected to the fullest extent of Indian law. Submission of this report does not constitute an admission that the medicine caused the reaction.

Section F — Review & Submit

Please review your report before submitting. You can go back to edit any section.

By submitting this report you confirm the information is accurate to the best of your knowledge. De-identified data may be submitted to CDSCO as required by Indian pharmaceutical law.

✅

Report Submitted Successfully!

Thank you for helping improve animal medicine safety across India. Your report has been received and will be reviewed by our pharmacovigilance team.

VT-ADE-XXXXXXXX

Save this reference number for your records

What happens next:

Acknowledgement email sent to you within 24 hours

Our team reviews your report within 48 hours

Serious reports are escalated immediately to our vet team

De-identified data may be submitted to CDSCO as required by law

Your identity is protected to the fullest extent of Indian law

Processed by

Vetnician Pharmacovigilance System

Indian Patent No. 561995 — System and Method for Veterinary Pharmacovigilance Monitoring and Recording

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