Acetaminophen (Tylenol / Paracetamol)
Analgesic and antipyretic metabolized primarily by the liver via glucuronidation and sulfation. Hepatotoxic in overdose.
Projected serum levels — 500 mg, as needed (shown daily)
Maintenance schedule: 500 mg as needed (shown daily) (oral).
Modeled steady state after ~1 days: peak ≈ 277 mg, trough ≈ 0.000 mg body load. Population-based estimate over 15 days for a 500 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Analgesic
- Route modeled
- Oral
- Model confidence
- predicted
- Half-life
- 2.3 h
- Common dose
- 500 mg
- Suggested maximum
- 4k mg/day
- Reference dose range
- 325–4k mg (single dose)
- Suggested cadence
- as needed (shown daily)
- Validated against
- 1k mg oral — Cmax 18 mg/L at 0.75 h
Documented interactions
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danger
Ethanol (Alcohol) + Acetaminophen (Tylenol / Paracetamol)
Alcohol induces CYP2E1, increasing toxic NAPQI metabolite formation from acetaminophen. High risk of liver failure.
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caution
1,4-BDO (1,4-Butanediol) + Acetaminophen (Tylenol / Paracetamol)
1,4-BDO conversion to GHB consumes ADH/ALDH capacity. Heavy or chronic dosing pulls on the same hepatic oxidation systems acetaminophen relies on for safe clearance, increasing NAPQI accumulation…
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moderate
CBD (Cannabidiol) + Acetaminophen (Tylenol / Paracetamol)
CBD (Cannabidiol) reversible_inhibitor of UGT1A9 predicted to change Acetaminophen (Tylenol / Paracetamol) AUC by ~1.28x
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watch
Efavirenz (Sustiva) + Acetaminophen (Tylenol / Paracetamol)
Efavirenz (Sustiva) inducer of CYP3A4 predicted to change Acetaminophen (Tylenol / Paracetamol) AUC by ~0.87x
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watch
Rifampin + Acetaminophen (Tylenol / Paracetamol)
Rifampin inducer of CYP3A4 predicted to change Acetaminophen (Tylenol / Paracetamol) AUC by ~0.87x
Serum checks 9 modeled interaction pairings for acetaminophen (tylenol / paracetamol) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Efficacy and safety of paracetamol for spinal pain and osteoarthritis: systematic review and meta-analysis of randomised placebo controlled trials
Meta-analysis found paracetamol was ineffective for low back pain and provided only small, clinically insignificant benefits for osteoarthritis pain and disability.
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Acetaminophen-induced hepatotoxicity: a comprehensive update
Review establishing acetaminophen overdose as the leading cause of acute liver failure in the US, detailing the NAPQI toxicity mechanism and NAC treatment.
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Paracetamol: not as safe as we thought? A systematic review of observational studies
Systematic review found dose-response relationship between paracetamol use and adverse events including increased cardiovascular, GI, and renal risks at higher doses.
3 published studies referenced in the app, each with a plain-language summary.