Acute Contrast Reaction: Documentation Form

Axial T2 brain MRI (MNI ICBM152 template) labelled: skull, white matter, grey matter, lateral ventricles. Handwritten note: CSF: bright on T2.
MRI: MNI ICBM152 2009b template. Copyright (C) 1993-2004 Louis Collins, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University. Labels added.

Acute Contrast Reaction: Documentation Form

For recording an acute reaction to iodinated or gadolinium-based contrast media. Severity categories harmonised with ACR, RCR/UK and ESUR guidance.

Updated September 2026

On this page1. Patient & study details2. Contrast agent administered3. Reaction type4. Severity (tick one): ACR / RCR / ESUR5. Observations at reaction6. Treatment given7. Outcome & disposition8. External adverse-reaction reporting9. Completed by
Not medical advice. Educational template only. Review and adapt against your local policy, drug formulary and resuscitation protocol before clinical use. In an emergency, follow your local anaphylaxis / resuscitation algorithm and call for help immediately.

1. Patient & study details

Patient name

ID / MRN

Date of birth

Weight (kg)

Date of reaction

Time of reaction

Examination / indication

Referring clinician

Location (scanner / room)

Relevant history (prior reaction, asthma, allergy, renal, cardiac, beta-blocker)

 

2. Contrast agent administered

Agent / trade name

Type

Dose (mL / mmol)

Concentration

Route

Injection rate

Batch / lot no.

Expiry

Time of injection

Onset after injection

Premedication given? (drug / dose / time)

3. Reaction type

Allergic-like

  • Urticaria / itching
  • Erythema / flushing
  • Angio-oedema (facial / lip / periorbital)
  • Throat tightness / hoarseness
  • Bronchospasm / wheeze
  • Stridor / laryngeal oedema
  • Anaphylaxis

Physiologic

  • Nausea / vomiting
  • Flushing / warmth / chills
  • Headache / dizziness / anxiety
  • Vasovagal (bradycardia + hypotension)
  • Hyper- / hypotension
  • Chest pain / arrhythmia
  • Seizure / convulsion

Extravasation? Volume / site / management

4. Severity (tick one): ACR / RCR / ESUR

Mild: self-limited, no progression

Mild reaction

Limited urticaria / itching, limited cutaneous oedema, “scratchy” throat, nasal congestion, sneezing, mild nausea/vomiting, transient flushing/warmth, mild headache/dizziness, self-limited vasovagal. Usually observation ± reassurance.

Moderate: more pronounced, may progress

Moderate reaction

Diffuse urticaria, facial oedema without dyspnoea, throat tightness without dyspnoea, mild bronchospasm/wheeze, protracted vomiting, hypertensive urgency, vasovagal needing treatment. Requires treatment and monitoring.

Severe: life-threatening

Severe reaction

Diffuse / facial oedema with dyspnoea, laryngeal oedema with stridor/hypoxia, bronchospasm with significant hypoxia, anaphylactic shock (hypotension + tachycardia), hypotension with allergic signs, vasovagal resistant to treatment, arrhythmia, seizures, cardiopulmonary arrest. Emergency: adrenaline, call resus team.

5. Observations at reaction

Time

GCS / consciousness

BP

Heart rate

Resp rate

SpO₂ (%)

Temperature

Peak flow (if done)

6. Treatment given

  • Stopped injection / removed cause
  • Called for help / resus team (2222 / code)
  • Airway support / positioning
  • High-flow oxygen, rate: __________
  • IM adrenaline 0.5 mg (0.5 mL 1:1000), time: ______
  • IV fluids (crystalloid), volume: __________
  • Salbutamol / bronchodilator
  • H1 antihistamine (e.g. chlorphenamine)
  • Hydrocortisone
  • Atropine (vasovagal / bradycardia)
  • Anti-emetic
  • Other: __________________________

Drugs / doses / times (free text)

 

7. Outcome & disposition

  • Full recovery on site
  • Observed, duration: __________
  • Referred to ED / admitted
  • Discharged with advice
  • Patient informed of reaction
  • GP / referrer notified

Follow-up / discharge advice given

Recommendation for future contrast (avoid / alternative agent / premedication)

Incident / clinical governance report filed?

Yellow Card / MHRA reported? (if applicable)

8. External adverse-reaction reporting

Report suspected reactions to your national pharmacovigilance body. Tick the one used and record the reference number returned.

  • New Zealand (CARM / Medsafe): report to the Centre for Adverse Reactions Monitoring (report-a-problem via medsafe.govt.nz, or nzphvc.otago.ac.nz; email nzphvc@otago.ac.nz)
  • UK (MHRA Yellow Card): yellowcard.mhra.gov.uk
  • Australia (TGA): tga.gov.au (Adverse Medicines Event Line 1300 134 237)
  • USA (FDA MedWatch): fda.gov/medwatch
  • Other / EU national authority: ______________________________

Reported by

Date reported

Reference / report number

Manufacturer notified? (batch recall)

9. Completed by

Name

Role / grade

Signature

Date & time

Supervising radiologist / clinician informed (name & time)

Severity framework harmonised from the ACR Manual on Contrast Media, the RCR (UK) standards for intravascular contrast, and the ESUR Contrast Media Safety Committee Guidelines 2025. Treatment doses shown are typical adult examples. Always follow your local resuscitation and anaphylaxis protocol and current drug formulary.

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