Data extraction form
| Study ID | |
| Title | |
| Author | |
| Country of study conduct | USA UK Canada Australia Other |
| Study characteristics | |
| Aim | |
| Design | RCT Non-randomised experimental study Cohort study Cross-sectional study Case–control study Systematic review Qualitative study Prevalence study Case series Case report Diagnostic test accuracy study Clinical prediction rule Economic evaluation Text and opinion Other |
| Start date | |
| End date | |
| Funding source | |
| Conflict of interest | |
| Participant characteristics | |
| Population description | |
| Inclusion criteria | |
| Exclusion criteria | |
| Sample size (n) | |
| Birth weight (g) | |
| Gestational age (week) | |
| Postnatal age (week) | |
| Underlying condition | |
| Comorbidities | |
| Concurrent medications | |
| Intervention/exposure details | |
| Paracetamol dosing regimen (mg/kg/dose) | |
| Paracetamol duration (days) | |
| Paracetamol route of administration | |
| Control details | |
| Pharmacotherapy | Sedative-analgesic Epidural NSAID Other |
| Non-specified standard treatment | |
| Outcomes | |
| Primary outcomes | |
| Long-term adverse effects | |
| Neurodevelopmental adverse events | |
| Atopic disorders | |
| Reproductive disorders | |
| Others | |
| Secondary outcomes | |
| Pharmacokinetic data | |
| Pharmacodynamic data | |
| Short-term adverse events | |
| Increased hepatic transaminases | |
| Gastrointestinal haemorrhage | |
| Necrotising enterocolitis | |
| Feeding intolerance | |
IQ, intelligence quotient; NSAID, non-steroidal anti-inflammatory drug; RCT, randomised controlled trial.