Effect of Histamine H2-receptor Antagonists on. Acetaminophen and its Metabolites in Human Plasma

Similar documents
PRODUCT INFORMATION Panadeine EXTRA

Bioequivalence Studies of Two Formulations of Famciclovir Tablets by HPLC Method

PRODUCT INFORMATION CODAPANE XTRA Paracetamol 500 mg and Codeine Phosphate 15 mg Tablets

SCHEDULING STATUS: S0 For pack sizes of 24 tablets or less. For pack sizes of more than 24 tablets

Short Communication. Abstract. Introduction

PARACOD Tablets (Paracetamol + Codeine phosphate)

Farmadol. Paracetamol 10 mg/ml INFUSION SOLUTION

Metabolism Paracetamol is metabolised in the liver and excreted in the urine mainly as glucuronide and sulphate conjugates.

GI Pharmacology. Dr. Alia Shatanawi 5/4/2018

PROFESSIONAL INFORMATION

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Molecular formula: Molecular weight: C 8 H 9 NO 2 CAS Registry no.:

AROMASIN 25mg (Tablets)

Passage of paracetamol into breast milk and its subsequent metabolism by the neonate

The dependence of paracetamol absorption on the rate of gastric emptying

NEW ZEALAND DATASHEET

A simple validated RP-HPLC method for quantification of sumatriptan succinate in bulk and pharmaceutical dosage form

Body weight more than 30kg : 10ml (10mg) of the syrup once daily.

Ranitidine hydrochloride syrup containing 150mg Ranitidine per 10mL

PACKAGE INSERT TEMPLATE FOR PARACETAMOL SUPPOSITORIES

SUCRALFATE ISELPIN 1 g Tablet

SUMMARY OF PRODUCT CHARACTERISTICS

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Panadeine Tablet, Caplets and Rapid Soluble tablets PRODUCT INFORMATION

Summary of Product Characteristics

Composition: Each tablet contain. Levocetirizine. Each 5ml contains. Montelukast. Pharmacokinetic properties:

The usual dose is 40 mg daily with amoxycillin 1.5 g (750 mg b.d.) for 2 weeks. Up to 2 g/day of amoxycillin has been used in clinical trials.

* Adults. NSAID associated peptic ulceration: - Acute treatment: 150 mg twice daily for 8 to 12 weeks, or 300mg nocte.

SUCRALFATE TABLETS, USP

PDF hosted at the Radboud Repository of the Radboud University Nijmegen

A. Incorrect! Histamine is a secretagogue for stomach acid, but this is not the only correct answer.

2. QUALITATIVE AND QUANTITATIVE COMPOSITION. Each capsule contains PARACETAMOL 500mg For a full list of excipients, see section 6.1.

Levocetirizine dihydrochloride

VALIDATED RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF DEXAMETHASONE AND GRANISETRON IN COMBINED DOSAGE FORMS

Evolution continues. Year: 1940 Fuel: Electricity Speed: 32 km/h. Year: 1998 Fuel: Electricity Speed: 118 km/h

NOTOPAIN CAPLETS. Diclofenac Sodium + Paracetamol. Composition. Each tablet contains: Diclofenac Sodium BP 50mg Paracetamol BP 500mg.

Osnove farmakokinetike. Aleš Mrhar. Prirejeno po. A First Course in Pharmacokinetics and Biopharmaceutics by David Bourne,

PRUCAPLA Tablets (Prucalopride)

SUCRALFATE TABLETS, USP

ISSN: ; CODEN ECJHAO E-Journal of Chemistry 2011, 8(3),

DOMCET Tablet / Suspension (Domperidone maleate + Paracetamol)

PARACIP Injection (Paracetamol )

Action Rufenal contains a non - steroidal compound with pronounced antirheumatic, anti-inflammatory, analgesic and antipyretic properties.

Preliminary studies of the pharmacokinetics and pharmacodynamics

Acetaminophen. TIP Session IV

DATA SHEET. PANADOL Mini Caps Capsule shaped tablet with a gelatin coating which is one half green and the other half white.

AUSTRALIAN PRODUCT INFORMATION PANADOL OPTIZORB TABLETS (PARACETAMOL) TABLETS PANADOL OPTIZORB CAPLETS (PARACETAMOL) TABLETS

COMPOSITION. A film coated tablet contains. Active ingredient: irbesartan 75 mg, 150 mg or 300 mg. Rotazar (Film coated tablets) Irbesartan

PANADOL COLD & FLU MAX HOT LEMON Powder for Oral Solution DATA SHEET

NEW ZEALAND DATA SHEET

Review article: pharmacology of esomeprazole and comparisons with omeprazole

EFFECTS OF MICROSOMAL ENZYME INDUCTION ON PARACETAMOL METABOLISM IN MAN

Introductionn Ilaprazole (ILA) is

Each 5ml of Sinarest LP New Syrup contains: Phenylephrine

Nizatidine Enhances the Gastrocolonic Response and the Colonic Peristaltic Reflex in Humans

Data Sheet. BICALOX 50 mg is a white to off-white, round, film coated, biconvex tablets, engraved with 'BC 50' on one face and plain on the other.

EXCRETION OF PARACETAMOL AND ITS METABOLITES IN MAN

Pharmacokinetics of ibuprofen in man. I. Free and total

HPLC-UV Determination of Abacavir Sulphate in Pharmaceutical Dosage Forms

SUMMARY OF PRODUCT CHARACTERISTICS

A HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC ASSAY FOR LERCANIDIPINE HYDROCHLORIDE

EMILOK Global. (omeprazole) Composition: Each capsule contains 20 mg omeprazole as enteric-coated

PANADOL EXTRA PRODUCT INFORMATION

Gastrointestinal side effects after intravenous erythromycin

Introduction to. Pharmacokinetics. University of Hawai i Hilo Pre-Nursing Program NURS 203 General Pharmacology Danita Narciso Pharm D

Children Enteric coated tablet : 1-3 mg/kg per day in divided doses.

OFIRMEV a non-opioid, non-nsaid, intravenous analgesic for the management of pain

Ausfam PRODUCT INFORMATION NAME OF THE MEDICINE DESCRIPTION PHARMACOLOGY

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

J Pharm Sci Bioscientific Res (4): ISSN NO

IUPAC Name 2-diethylaminoethyl 1- cyclohexylcyclohexane-1- carboxylate Chemical Structure. Molecular Weight

RISK MANAGEMENT PLAN (RMP) PUBLIC SUMMARY ETORICOXIB ORION (ETORICOXIB) 30 MG, 60 MG, 90 MG & 120 MG FILM-COATED TABLET DATE: , VERSION 1.

1. The proposed strength, quantity, dosage form, dose and route of administration of the medicine including indication

SUMMARY OF PRODUCT CHARACTERISTICS

Pharmacokinetics of intravenous and oral salbutamol and its sulphate conjugate

PANADOL OSTEO PRODUCT INFORMATION

Hyderabad, India. Department of Pharmaceutical Chemistry, Glocal University, Saharanpur, India.

Results. Subject Disposition and Demographics Of 37 enrolled subjects, 23 (62.2%) completed the study

NEW ZEALAND DATA SHEET

RP-HPLC Analysis of Temozolomide in Pharmaceutical Dosage Forms

Acilight 75mg Tablets. Ranitidine Hydrochloride 83.57mg eq.to Ranitidine 75mg. Generic Name: Ranitidine Hydrochloride 83.57mg eq.

Effective pain management begins with OFIRMEV (acetaminophen) injection FIRST Proven efficacy with rapid reduction in pain 1

TERICOX. Composition Each film-coated tablet contains 60, 90, or 120 mg of Etoricoxib.

CHILDREN S PANADOL COLOURFREE SUSPENSION PANADOL SUPPOSITORIES 125 MG PANADOL SUPPOSITORIES 250 MG DATA SHEET. Proprietary (Trade) Name: PANADOL

M0BCore Safety Profile

Validated RP-HPLC Method for the Estimation of Esomeprazole Enteric Coated Tablets

Summary of Product Characteristics

Section 5.2: Pharmacokinetic properties

Gastric, intestinal and colonic absorption of metoprolol in

Summary of Product Characteristics

SIMULTANEOUS ESTIMATION OF VALSARTAN AND HYDROCHLOROTHIAZIDE IN TABLETS BY RP-HPLC METHOD

Domperidon Betapharm 10 mg tablets. Summary of Product Characteristics. 1:(to be changed into local product name in each CMS after day 90)

Patient leaflet: Information for the user. Paracetamol Galpharm 500mg tablets paracetamol

PRODUCT INFORMATION LEAFLET

Reflux of gastric contents, particularly acid, into the esophagus

All pharmacodynamic effects observed can be explained by the effect of omeprazole on acid secretion.

Click to edit Master title style

JYNARQUE REMS (RISK EVALUATION AND MITIGATION STRATEGY) PATIENT GUIDE

Transcription:

Jpn. J. Pharm. Health Care Sci. Effect of Histamine H2-receptor Antagonists on Acetaminophen and its Metabolites in Human Plasma Hiroki Itoh* and Masaharu Takeyama Department of Clinical Pharmacy, Oita University Hospital Received October 17, 2003 Accepted November 14, 2003 The effect of histamine H2-receptor antagonists on plasma concentrations of acetaminophen was investigated with respect to hepatic metabolism. Acetaminophen (1000 mg) was administered orally together with ranitidine (300 mg), nizatidine (300 mg), nizatidine (150 mg) or placebo to five healthy male volunteers. Venous blood samples were taken before and after administration and plasma acetaminophen and acetaminophen conjugates (glucuronide and ) were measured by high-performance liquid chromatography. The pharmacokinetic parameters were calculated from the plasma acetaminophen concentration-time curves for each volunteer. With ranitidine, compared with placebo, plasma acetaminophen concentrations were significantly increased from 15 to 120 min. and plasma acetaminophen glucuronide conjugate concentrations were significantly decreased from 15 to 45 min. With nizatidine, as compared with placebo, plasma acetaminophen concentrations were significantly increased from 45 to 120 min. and 45 to 60 min. for the high and low doses of the drug, respectively. Acetaminophen glucuronide concentrations were significantly decreased from 30 to 45 min. and at 30 min., respectively, for the high and low doses of nizatidine, respectively. However, with ranitidine and nizatidine, plasma acetaminophen concentrations were not significantly altered. Co-administration with ranitidine or nizatidine reduces plasma acetaminophen glucuronide concentrations and increases plasma acetaminophen concentrations dose-dependently. These effects of ranitidine and nizatidine could result from inhibition of glucuronyltransferase. Therefore, care is necessary when administering acetaminophen together with ranitidine or nizatidine. Key words \acetaminophen, ranitidine, nizatidine, metabolism Introduction Acetaminophen has analgesic and antipyretic effects and is widely used to treat pain and fever. The side-effects are hepatitis, renal failure, agranulocytosis, anaemia, dermatitis, allergy, sterile pyuria and thrombocytopenia1). Acetaminophen is poorly absorbed from the stomach, but rapidly absorbed from the small intestine. The major metabolic pathways of a therapeutic dose of acetaminophen in humans are glucuronidation and sulphation, which account for about 60 % and 30% of its metabolism, respectively2). Peak plasma concentrations are usually reached 30-60 min after oral administration, and the half-life in plasma is approximately 120 min in a therapeutic dose. However, acute overdosage causes fatal hepatic damage. The histamine H2-receptor antagonists, which are widely used clinically to treat peptic ulcers, gastroesophageal reflux diseases and gastritis, are potent inhibitors of gastric acid secretion3). The dysfunction of gastrointestinal motility is responsible for some upper abdominal symptoms, nausea, vomiting, dyspepsia and epigastric pain4). Histamine H2- receptor antagonist is frequently given in combination with acetaminophen. In this study, we examined the effects of histamine H2- receptor antagonists on acetaminophen metabolism by measuring the plasma concentrations of acetaminophen and its conjugates before and after administration of acetaminophen with ranitidine or nizatidine to five healthy male volunteers. Materials and Methods Acetaminophen (Calonal tablets, Showa Yakuhin Kako Co., Ltd., Tokyo, Japan), ranitidine (Zantac tablets ; Sankyo Co., Ltd, Tokyo, Japan) and nizatidine (Acinon capsules, Zeria Pharmaceutical Co., Ltd., Osaka, Japan) were used. Lactose (Merck hoei Co., Ltd., Osaka, Japan) was used as placebo. Standard acetaminophen and acetaminophen glucuronide were purchased from Sigma chemical Co. (St. Louis,

68 MO). Standard acetaminophen was supplied by Hokuriku Seiyaku Co., Ltd. (Fukui, Japan). All other reagents were of analytical reagent grade from commercial sources. 2. Subjects Five healthy male volunteers, aged 23-29 years (median 26 years), weighing 55-68 kg (median 62 kg), participated in the study. Each subject received information about the scientific purpose of the study, which was approved by our Ethics Committee at Oita University, and gave informed consent. The subjects did not receive any medication one week before the study, and fasted for 12 h before the study commenced and during the experiments. 3. Study schedule Acetaminophen (1000 mg) together with ranitidine (300 mg), nizatidine (300 mg), nizatidine (150 mg) or placebo were administered orally with 100 ml water. Each subject was administered these drugs at an interval of three weeks. The dose of ranitidine and nizatidine in this study was the same as a daily dose in clinical therapy. Venous blood samples (10 ml) were taken from a forearm vein before and at 15, 30, 45, 60, 90, 120 and 180 min after acetaminophen administration. This study was carried out from 0800 to 1100 h. 4. Determination of acetaminophen and acetaminophen metabolites The concentrations of acetaminophen, acetaminophen glucuronide and acetaminophen were determined by the modified method of Mineshita et al5) and Brunner & Bai6). The plasma samples were deproteinized with 5% perchloric acid and centrifuged at 5000 g for 2 min. The supernatant was filtered through a membrane filter (Sample 4-LH, 0.45 and then applied onto high-performance liquid chromatography (HPLC). HPLC was carried out using a C18 column (Cosmosil 5C 18-AR, Nacalai Tesque) at 45 with UV detection at 254 nm. The mobile phase was 1% acetic acid/0.1 M potassium dihydrogen phosphate (3 : 97), at a flow rate of 1.0 ml/min. The recovery of acetaminophen, acetaminophen glucuronide and acetaminophen in plasma using this extraction procedure was 91.8 Results The concentration-time curves of acetaminophen, acetaminophen glucuronide and acetaminophen in plasma from the five male volunteers are shown in Figure 1-6. Mean peak plasma acetaminophen concentrations were significantly elevated from 18.3 } 2.3 ƒêg/ml (placebo-coadministration) to 34.1 } 1.1 ƒêg/ml (ranitidine-coadministration) 30 min after administration (P ƒ 0.01). Plasma acetaminophen concentrations were increased significantly at 15 to 120 min (P ƒ 0.01). The AUC of acetaminophen was increased 1889.0 } 132.6 ƒêg min/ml (placebo-coadministration) to 2819.9 } 32.2 ƒêg min/ml (ranitidine-coadministration) (P ƒ 0.01) (Fig. 1). The plasma acetaminophen glucuronide with ranitidine was significantly reduced at 15 to 45 min compared with placebo (P ƒ 0.01) (Fig. 2). Plasma acetaminophen concentrations with ranitidine were not significantly changed after administration compared with placebo (Fig. 3). 2. Effects of nizatidine (300 mg) on plasma concentrations Mean peak plasma acetaminophen concentartions were elevated from 18.3 } 2.3 ƒêg/ml (placebo-coadministration) to 21.0 } 2.8 ƒêg/ml (nizatidine-coadministration) 30 min after administration. Plasma acetaminophen concentrations with nizatidine were increased significantly at 45 to 120 min (P ƒ 0.01). The AUC of acetaminophen was increased 1889.0 } 132.6 ƒêg min/ml (placebo-coadministration) to 2361.5 } 146.4 ƒêg min/ml (nizatidine-coadministration) (P The plasma acetaminophen glucuronide with nizatidine was significantly reduced at 30 to 45 min concentrations of acetaminophen, acetaminophen glucuronide and acetaminophen were proportional to the peak area over the range 1.0-100, 1.0-200 and 1.0-150 ƒêg/ ml, respectively. 5. Statistical analysis All values are expressed as means } sd. The area under the plasma concentration-time (0-180 min) curve (AUC) was calculated using the trapezoidal method. Comparison of mean values were made by one-way analysis of variance and P ƒ 0.05 was considered statistically significant. Fig. 1. Plasma Acetaminophen Concentrations after Coadministration of Ranitidine ( œ), or Placebo value represents the mean } s.d. of concentrations in five volunteers. * *P ƒ 0.01 significantly different compared with placebo.

69 Fig.4. Plasma Acetaminophen Concentrations after Coadministration of 300 mg Nizatidine ( œ) and 150 mg Nizatidine ( ), Placebo ( ). Each Fig. 2. Plasma Acetaminophen Glucuronide Concentrations after Coadministration of Ranitidine ( œ), or Placebo ( ). Each value represents the value represents the mean s.d. of concentrations in five volunteers. * *P ƒ 0.01 significantly different compared with placebo. mean } s.d. of concentrations in five volunteers. significantly different compared with placebo. Fig. 5. Plasma Acetaminophen Glucuronide Concentrations after Coadministration of 300 mg Nizatidine ( œ) and 150 mg Nizatidine (111), Placebo ( ). Each value represents the mean s.d. of concentrations in five volunteers. *P ƒ 0.05 and * *P ƒ 0.01 significantly different compared with placebo. Fig. 3. Plasma Acetaminophen Sulphate Concentrations after Coadministration of Ranitidine ( œ), or Placebo ( ). Each value represents the mean } s.d. of concentrations in five volunteers. compared with placebo (P ƒ 0.01) (Fig. 5). Plasma acetaminophen concentrations with nizatidine were not significantly changed after administration compared with placebo (Fig. 6). 3. Effects of nizatidine (150 mg) on plasma concentrations Mean peak plasma acetaminophen concentartions were elevated from 18.3 } 2.3 ƒêg/ml (placebo-coadministration) to 20.2 } 0.9 ƒêg/ml (nizatidine-coadministration) 30 min after administration. Plasma acetaminophen concentrations Fig. 6. Plasma Acetaminophen Sulphate Concentrations after Coadministration of 300 mg Nizatidine Each value represents the mean } s.d. of concentrations in five volunteers. with nizatidine were increased significantly at 45 to 60 min (P ƒ 0.01). The AUC of acetaminophen was increased 1889.0 } 132.6 ƒêg min/ml (placebo-coadministration) to 2085.8 } 73.5 ƒêg min/ml (nizatidine-coadministration) (P with nizatidine was significantly reduced at 30 min compared with placebo (P ƒ 0.05) (Fig. 5). Plasma aceta-

70 minophen concentrations with nizatidine were not significantly changed after administration compared with placebo (Fig. 6). Discussion Coadministration of acetaminophen with ranitidine or nizatidine increased acetaminophen concentrations and delayed acetaminophen glucuronide transformation. We found a pharmacokinetic interaction between acetaminophen and ranitidine or nizatidine when both drugs were coadministered. Acetaminophen is clinically effective as an analgesic and antipyretic treatment. Its absorption appears to be negligible from the stomach, but very rapid from the small intestine. The conventional oral dose of acetaminophen is 300-500 mg, with a total daily dosage not exceeding 1.5 g. Although acetaminophen produces fewer side-effects than aspirin in therapeutic doses, skin rashes and other allergic reactions occur occasionally1). Acetaminophen is mainly metabolized by the liver to glucuronide and conjugates. The histamine H2-antagonists are widely used as an effective therapy for peptic ulcer diseases, gastroesophageal reflux diseases, gastritis and hyper-secretory states. Ranitidine and nizatidine have anti-acetylcholinesterase activity, and stimulate gastrointestinal motility and gastric emptyine. Emery et al8 reported that ranitidine caused 50% inhibition of glucuronide conjugation in cultured rat hepatocytes. Plasma concentrations of acetaminophen in rats after pretreatment with ranitidine were significantly increased compared with rats treated with acetaminophen alone9). Inhibition of acetaminophen glucuronyltransferase activity by ranitidine would reduce acetaminophen conjugation. Therefore we examined the effects of ranitidine and nizatidine on the hepatic metabolism of acetaminophen. The profiles of plasma acetaminophen, acetaminophen glucuronide and acetaminophen concentrations are indicated in Figure 1-6. In our study, plasma acetaminophen concentrations were affected by rantidine and nizatidine coadministration. Significant increases in peak plasma acetaminophen concentrations were found at 30 min with the coadministartion of ranitidine (1.9-times vs placebo). Plasma acetaminophen concentrations with ranitidine coadministration increased significantly from 15 to 120 min. Plasma acetaminophen glucuronide conjugate concentrations with ranitidine were decreased significantly at 15 to 45 min compared with placebo. Plasma acetaminophen conjugate concentrations did not change significantly. Thus, plasma acetaminophen concentrations would be increased in the process of absorption in the presence of ranitidine. Coadministration of ranitidine significantly increased the AUC of acetaminophen (approx. 1.6-times compared with placebo). This was probably due to the prevention of acetaminophen glucuronyltransferase by ranitidine9). Coadministration of nizatidine significantly increased plasma acetaminophen concentrations and the AUC of acetaminophen. Nizatidine at dose of 150 and 300 mg significantly increased the AUC of acetaminophen to 2085.8 } 73.5 and 2361.5 } 146.4 Đg E min/ml, respectively, in a dosedependent manner. Plasma acetaminophen glucuronide concentrations with nizatidine (300 and 150 mg) were decreased significantly at 30-45 min and 30 min, respectively. This study showed the coadministration of acetaminophen with ranitidine and nizatidine causes a dose-dependent, significant decrease in plasma acetaminophen glucuronide concentrations and increases in plasma acetaminophen concentrations. Thus, ranitidine and nizatidine may prevent the first-pass hepatic metabolism of acetaminophen and delay the extent of acetaminophen glucuronyltransferase activity during the process of absorption in the presence of ranitidine and nizatidine. The same effect was confirmed with cimetidine, not famotidine (data not shown). These findings are potentially important clinically, particularly if ranitidine and nizatidine can increase the toxicity of acetaminophen. Drugs become commercially available after non-clinical and clinical studies, but processes that take place after marketing are also important for pharmaceutical development. This type of study is extremely important and useful to clinicians and pharmacists10,11). From the viewpoint of postmarketing development, we are in the process of establishing indicators for the proper usage of pharmaceutical drugs. References 1) S.P. Clissold, Paracetamol and phenacetin, Drug., 32 (suppl 4), 46-59 (1986). 2) J. Shibasaki, T. Koizumi, T. Tanaka, Drug Absorption, Metabolism, and Excretion. I. Some Pharamacokinetic Aspects of Metabolism of Acetanilide 4-Hydroxyacetanilide, Chem. Pharm. Bull., 16, 1661-1673 (1968). 3) T.M. Lin, D.C. Evans, M.W. Warrick, R.P. Pioch, Actions of nizatidine, a selective histamine H2-antagonist, on gastric acid secretion in dogs, rats and frogs, J. Pharmacol. Exp. Ther., 239, 406-410 (1986). 4) S. Ueki, M. Seiki, T. Yoneta, H. Aita, K. Chaki, Y. Hori, H. Morita, E. Tagashira, Z. Itoh, Gastroprokinetic activity of nizatidine, a new H2-receptor antagonist, and its possible mechanism of action in dogs and rats, J. Pharmacol. Exp. Ther., 264, 152-157 (1992). 5) S. Mineshita, R. Eggers, N.R. Kitteringham, E.E. Ohnhaus, Determination of phenacetin and its major metabolites in human plasma and urine by highperformance liquid chromatography, J. chromatogr., 380, 407-413 (1986). 6) L.J. Brunner, S. Bai, Simple and rapid assay for acetaminophen and conjugated metabolites in low-volume serum samples, J. Chromatogr. B., 732, 323-329 (1999). 7) R.C. Heading, J. Nimmo, L.F. Prescott, P. Tothill, The dependence of paracetamol absorption on the rate of gastric emptying, Brit. J. Pharmac.,.47, 415-421

(1973). 8) S. Emery, H.G. Oldham, S.J. Norman, R.J. Chenery, The effect of cimetidine and ranitidine on paracetamol glucuronidation and sulphation in cultured rat hepatocytes, Biochem. Pharmacol., 34, 1415-1421 (1985). 9) S.A. Rogers, K.C. Gale, J.F. Newton, J.G. Dent, T.B. Leonard, Inhibition by ranitidine of acetaminophen conjugation and its possible role in ranitidine potentiation of acetaminophen-induced hepatotoxicity, J. Pharmacol. Exp. Ther., 245, 887-894 (1988). 10) H. Itoh, T. Nagano, T. Hayashi, M. Takeyama, Ranitidine increases bioavailability of acetaminophen by inhibiting first-pass glucuronidation in man, Pharm. Pharmacol. Commun., 6, 495-500 (2000). 11) H. Itoh, T. Nagano, T. Hayashi, M. Takeyama, Effect of nizatidine on paracetamol and its metabolites in human plasma, J. Pharm. Phamacol., 54, 869-873 (2002).