Acetaminophen (Systemic)
Acetaminophen (Systemic)
Acetaminophen (Systemic)
Acetaminophen (Systemic)
Introductory Information
Synthetic nonopiate derivative of p-aminophenol; produces analgesia and antipyresis.198, 207, 222
Brands*: Acephen®, Anacin® Aspirin Free Extra Strength, Axocet® (combination), Bupap®
(combination), Capital® and Codeine (combination), Ceta-Plus® (combination), Co-Gesic®
(combination), Endocet® (combination), Epidrin® (combination), Esgic-Plus® (combination),
Excedrin® Extra Strength (combination), Excedrin® Migraine (combination), Excedrin PM®
(combination), FeverAll®, Fioricet® (combination), Fioricet® with Codeine (combination), Gelpirin®
(combination), Genapap®, Genebs®, Goody's® (combination), Hydrogesic® (combination), Lorcet®
(combination), Lortab® (combination), Maxidone® (combination), Midol® Menstrual Complete
Maximum Strength (combination), Midol® Teen Menstrual Formula (combination), Midrin®
(combination), Ornex® (combination), Pamprin® Cramp (combination), Pamprin® Multi-Symptom
(combination), Percocet® (combination), Percogesic® (combination), Phrenilin® (combination),
Premsyn PMS® (combination), Roxicet® (combination), Sedapap® (combination), Tylenol®,
Tylenol® Extra Strength (combination), Tylenol® with Codeine (combination), Tylenol® PM Extra
Strength (combination), Tylox® (combination), Ultracet® (combination), Vanquish® (combination),
Vicodin® (combination), Zydone® (combination)
Special Alerts:
[Posted 01/13/2011] ISSUE: FDA notified healthcare professionals that it has asked drug
manufacturers to limit the strength of acetaminophen in prescription drug products, predominantly
combinations of acetaminophen and opioids, to 325 mg per tablet, capsule, or other dosage unit,
making these products safer for patients. This action will help to reduce the risk of severe liver injury
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and allergic reactions associated with acetaminophen. A Boxed Warning highlighting the potential for
severe liver injury and a Warning highlighting the potential for allergic reactions (swelling of the face,
mouth, and throat, difficulty breathing, itching, or rash) will be added to the label of all prescription
drug products that contain acetaminophen.
BACKGROUND: Acetaminophen, one of the most commonly used drugs in the United States, is
widely and effectively used in both prescription and over-the-counter (OTC) products to reduce pain
and fever. Examples of prescription products that contain acetaminophen include hydrocodone with
acetaminophen (Vicodin, Lortab), and oxycodone with acetaminophen (Tylox, Percocet). OTC
products containing acetaminophen (e.g., Tylenol) are not affected by this action. Information about
the potential for liver injury is already required on the label for OTC products containing
acetaminophen. FDA is continuing to evaluate ways to reduce the risk of acetaminophen related liver
injury from OTC products. No drug shortages are expected, because the 3-year implementation period
should permit adequate time for necessary reformulations.
RECOMMENDATION: Healthcare professionals were reminded to advise patients not to exceed the
acetaminophen maximum total daily dose (4 grams/day), and not to drink alcohol while taking
acetaminophen-containing medications.
Healthcare professionals were encouraged to inform patients that there is no immediate danger to
patients who take these combination pain medications, and patients should continue to take them as
directed by their health care provider. The Drug Safety Communication provides additional
information for healthcare professionals, information for patients, a data summary and a list of all
affected products. For more information visit the FDA website at: [Web] and [Web].
Uses
Pain
Self-medication in children ≥6 years of age and adults for the temporary relief of minor aches and pain
associated with headache, muscular aches, backache, minor arthritis pain, common cold, toothache, and
menstrual cramps.222 Self-medication in infants and children for the temporary relief of minor aches and
pain associated with the common cold, flu, headache, sore throat, immunizations, toothache, muscle
aches, sprains, and overexertion.207, 235
Self-medication in fixed combination with aspirin and caffeine for the temporary relief of mild to
moderate pain associated with migraine headache.212, 213, 214 This combination also can be used for the
treatment of severe migraine headache if previous attacks have responded to similar nonopiate
analgesics or NSAIAs.231
Symptomatic treatment of pain associated with osteoarthritis; considered an initial drug of choice for
pain management in osteoarthritis patients.197, 199, 200, 201
Used in fixed combination with isometheptene and dichloralphenazone for symptomatic relief of tension
and vascular headaches.251, 252
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Fever
Administration
Usually administered orally; may be administered rectally as suppositories in patients who cannot
tolerate oral therapy.207, 222, 226, 227, 228
Oral Administration
Swallow extended-release tablets whole; do not crush, chew, or dissolve in liquid.222
Because combinations and dosage strengths vary for fixed-combination preparations, consult
manufacturer's product labeling for appropriate dosage of the specific preparation.
Pediatric Administration
Acetaminophen oral drops generally used in infants 0-23 months of age.207 Use the calibrated dosing
device provided by the manufacturer for measurement of the dose.207
Oral suspension may be used in children ≥4 months age.207 Use the calibrated dosage cup provided by
the manufacturer for measurement of the dose.207
80-mg chewable tablets or orally disintegrating tablets may be used in children ≥2 years of age.207, 235
160-mg chewable tablets or orally disintegrating tablets or 325-mg conventional tablets commonly used
in children ≥6 years of age.207, 222, 235
Orally disintegrating tablets (Tylenol® Meltaways) should be allowed to dissolve in the mouth or should
be chewed before swallowing.237 Use caution to ensure that the correct number of tablets required for
the intended dose is removed from the blister package.236, 237
Rectal Administration
Dividing suppositories in an attempt to administer lower dosages may not provide a predictable dose.226
Some experts state that rectal acetaminophen preparations should not be used for self-medication in
children unless such use is specifically discussed with a clinician and parents or caregivers are instructed
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Dosage
Pending revision, the material in this section should be considered in light of more recently available
information in the MEDWATCH notification at the beginning of this monograph.
Pediatric Patients
Dosage in children should be guided by body weight.207, 237 (See Pediatric Use under Cautions.)
Pain
Oral:
For self-medication in children ≥12 years of age, 650 mg or 1 g every 4-6 hours as necessary (maximum
4 g daily).222
>Rectal
Fever
Oral:
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For self-medication in children ≥12 years of age, 650 mg or 1 g every 4-6 hours as necessary (maximum
4 g daily).222
>Rectal
Adults
Pain
Oral: For self-medication, 650 mg or 1 g every 4-6 hours as necessary (maximum 4 g daily).222
Alternatively, 1.3 g as extended-release tablets every 8 hours.222
>Rectal
325-650 mg every 4 hours as necessary.198
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Fever
Oral: For self-medication, 650 mg or 1 g every 4-6 hours as necessary (maximum 4 g daily).222
>Rectal
325-650 mg every 4 hours as necessary.198
Prescribing Limits
Pediatric Patients
Pain
Oral: Do not exceed recommended daily dosage.204, 205, 206, 207, 237 Self-medication should not exceed
5 days.207
Fever
Oral: Do not exceed recommended daily dosage.204, 205, 206, 207, 237 Self-medication should not exceed
3 days.207
Adults
Current limit is 4 g daily.197, 198, 222 Some experts recommend a maximum dosage of 3 g daily when
used for long-term therapy (e.g., ≥2 weeks).243 FDA is evaluating whether data exist to support
establishing a lower (i.e., <4 g daily) maximum daily dosage for certain patients (e.g., those who
chronically ingest alcohol).245, 246
Pain
>Oral or Rectal
Maximum 4 g daily.198, 222 Self-medication should not exceed 10 days.222
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Fever
>Oral or Rectal
Maximum 4 g daily.198, 222 Self-medication should not exceed 3 days.222
Cautions
Contraindications
Warnings/Precautions
Warnings
Hepatic Effects
Pending revision, the material in this section should be considered in light of more recently available
information in the MEDWATCH notification at the beginning of this monograph.
Ingestion of a single toxic dose or multiple excessive doses can result in hepatotoxicity.222, 223
Following suspected overdosage, evaluate necessity of antidote (acetylcysteine) therapy.222, 223, 225, 229
Increased serum ALT concentrations reported in healthy individuals receiving acetaminophen 4 g daily
for 14 days in 1 study.239
Sensitivity Reactions
Sensitivity reactions reported rarely.222 If such reactions occur, discontinue the drug.207, 222
Sulfite Sensitivity
Some formulations contain sulfites, which may cause allergic-type reactions (including anaphylaxis and
life-threatening or less severe asthmatic episodes) in certain susceptible individuals.a
General Precautions
Do not use multiple acetaminophen-containing preparations concomitantly.207, 222, 235
Phenylketonuria
Children's Tylenol® and Junior Strength Tylenol® chewable tablets contain aspartame (NutraSweet®),
which is metabolized in the GI tract to phenylalanine.207
When used in fixed combination with other agents (e.g., aspirin, caffeine, chlorpheniramine,
dextromethorphan, dichloralphenazone, diphenhydramine, doxylamine, guaifenesin, isometheptene,
phenylephrine, pseudoephedrine), consider the cautions, precautions, and contraindications associated
with the concomitant agent(s).212, 251, 252, 253, 254, 255, 256, 257, 258, 259
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Specific Populations
Pregnancy
Category B.b
Lactation
Distributed into milk;198 however, AAP considers acetaminophen to be usually compatible with breast-
feeding.250
Pediatric Use
Severe hepatotoxicity and death reported in children who apparently received acetaminophen dosages
exceeding those recommended202, 203, 204, 205, 206 (10-15 mg/kg per dose with a maximum of 5 doses
per day) for children.202, 204 Contributing factors include improper interpretation of dosing information
or failure to read such information, use of adult-strength preparations, use of excessive dosing because
of the perception that desired therapeutic effects had not been achieved, and lack of knowledge about the
potential toxicity of acetaminophen in excessive dosage.203, 204, 205, 206
Risk of overdosage and toxicity (including death) in children <2 years of age receiving preparations
containing antihistamines, cough suppressants, expectorants, and nasal decongestants alone or in
combination for relief of symptoms of upper respiratory tract infection.247, 248 Limited evidence of
efficacy for these cold and cough preparations in this age group; appropriate dosages not established.247
Therefore, FDA recommends not to use such preparations in children <2 years of age; safety and
efficacy in older children currently under evaluation. Because children 2-3 years of age also are at
increased risk of overdosage and toxicity, some manufacturers of oral nonprescription cough and cold
preparations recently agreed to voluntarily revise the product labeling to state that such preparations
should not be used in children <4 years of age. During the transition period, some preparations on
pharmacy shelves will have the new recommendation ("do not use in children <4 years of age"), while
others will have the previous recommendation ("do not use in children <2 years of age"). FDA
recommends that parents and caregivers adhere to dosage instructions and warnings on the product
labeling that accompanies the preparation and consult a clinician about any concerns.
Interactions
Specific Drugs
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Pharmacokinetics
Absorption
Bioavailability
Well absorbed following oral administration, with peak plasma concentration attained within 10-60
minutes (immediate-release preparations) or 60-120 minutes (extended-release preparations).a
Poor or variable absorption following rectal administration; considerable variation in peak plasma
concentrations attained; time to reach peak plasma concentration is substantially longer than after oral
administration.226, 227, 228
Food
Food may delay absorption following administration as extended-release tablets.148
Distribution
Extent
Rapidly distributed to most body tissues.a Crosses placenta and is distributed into breast milk.198
Elimination
Metabolism
Metabolized principally by sulfate and glucuronide conjugation; 226 small amounts (5-10%) oxidized by
CYP-dependent pathways (mainly CYP2E1 and CYP3A4) to a toxic metabolite, N-acetyl-p-
benzoquinoneimine (NAPQI).226 NAPQI is detoxified by glutathione and eliminated; any remaining
toxic metabolite may bind to hepatocytes and cause cellular necrosis.121, 226
Elimination Route
Mainly excreted in urine as conjugates.a
Half-life
1.25-3 hours.a
Special Populations
Following toxic doses or in patients with liver damage, plasma half-life may be prolonged.a
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In patients with moderate to severe renal impairment, acetaminophen conjugates may accumulate.a
Stability
Storage
Oral
Tablets
Room temperature.222 Protect orally disintegrating tablets (Tylenol® Meltaways) from high
humidity.235 Protect grape-flavored orally disintegrating tablets from light.235
Suspension/Solution
Room temperature.207
Actions
Advice to Patients
Pending revision, the material in this section should be considered in light of more recently available
information in the MEDWATCH notification at the beginning of this monograph.
• Risk of severe hepatic damage with use of excessive dosages, with concomitant use of multiple
acetaminophen-containing preparations, and in those consuming substantial amounts of alcohol (e.g.,
≥3 alcohol-containing drinks per day) concomitantly.245, 246
• When used for self-medication, importance of reading the product labeling.222 Importance of not
exceeding the recommended daily dosage204, 205, 206, 207, 235, 238, 245, 246 and of not using other
acetaminophen-containing products (e.g., some cold and cough products) concomitantly.204, 207, 235,
238, 245, 246
• When used for self-medication in pediatric patients, importance of basing the dose on the child's
weight;205, 207 importance of not exceeding the recommended daily dosage.204, 205, 206, 207, 235
• Importance of advising parents and caregivers about the appropriate dose, frequency, duration of
therapy, and specific strength and formulation for an individual pediatric patient.226 Advise of the
danger of substituting alternative dosage forms, particularly adult for pediatric formulations.226
• Importance of ensuring that the correct amount of medication required for the intended dose is
administered (e.g., importance of using only the calibrated measuring device provided with the
particular formulation for measuring the dose, importance of ensuring that the strength and number of
dosage units correspond to the intended dose).205, 207, 226, 236
• Importance of seeking quick medical attention if ingested dosage exceeds recommended dosage.207,
222, 235
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prescription and OTC drugs (e.g., cough/cold preparations) as well as any concomitant illnesses.
• Importance of informing patients of other important precautionary information. (See Cautions.)
Preparations
Excipients in commercially available drug preparations may have clinically important effects in some
individuals; consult specific product labeling for details.
Pending revision, the material in this section should be considered in light of more recently available
information in the MEDWATCH notification at the beginning of this monograph.
Acetaminophen
Routes Dosage Forms Strengths Brand Names Manufacturer
Bulk Powder
Oral Capsules 500 mg* Acetaminophen Capsules
167 mg/5
Solution
mL Tylenol® Extra-Strength Adult McNeil
100
mg/mL* Genapap® Drops Infant's Teva
Tablets, film-coated 500 mg* Anacin® Aspirin Free Extra Strength Insight
Tablets
Tylenol® Extra Strength Caplets McNeil
Tablets, orally disintegrating 80 mg Tylenol® Meltaways Children's McNeil
160 mg Tylenol® Meltaways Junior Strength McNeil
Rectal Suppositories 80 mg FeverAll® Infants' Alpharma
120 mg* Acephen® G&W
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Oral Suspension
120 mg/5 mL Acetaminophen and Capital® and Codeine Actavis
Codeine Phosphate 12 mg/5 mL (combination) (C-V)
300 mg Acetaminophen and Acetaminophen and Codeine
Tablets
Codeine Phosphate 15 mg* Phosphate Tablets (C-III)
300 mg Acetaminophen and Tylenol® with Codeine No. 3 Ortho-
Codeine Phosphate 30 mg* (combination) (C-III) McNeil
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Oral
Tablets, film- 500 mg Acetaminophen and Excedrin PM® Caplets Novartis
coated Diphenhydramine Citrate 38 mg (combination)
Excedrin PM® Geltabs Novartis
(combination)
Excedrin PM® Tablets Novartis
(combination)
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Solution
167 mg/5 mL with Hydrocodone Lortab® Elixir (combination) UCB Pharma
Bitartrate 2.5 mg/5 mL* (C-III)
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Comparative Pricing
This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing
information was updated 10/2011. For the most current and up-to-date pricing information, please visit
www.drugstore.com. Actual costs to patients will vary depending on the use of specific retail or mail-
order locations and health insurance copays.
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Tylenol Arthritis Pain 650MG Controlled-release Tablets (MCNEIL CONSUMER): 100/$22.99 or 200/
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$34.97
References
Only references cited for selected revisions after 1984 are available electronically.
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