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  Peginterferon alfa-2a
  Ribavirin
Herbs with Drug Interactions - a Partial List
 
  A western MD's view of the use of herbs by patients with HCV

Does Use of Complementary Treatments with Peginterferon plus Ribavirin Combination Therapy Provide a Benefit to Patients with Chronic Hepatitis C?

 

  Daily Cannabis Smoking as a Risk Factor for Fibrosis Progression in Chronic HCV

 (06/06/06)

DDW: Smoking Cigarettes Reduced SVR Rates in Peg/RBV Study -


AASLD: Smoking Marijuana Raises Fibrosis Risk in Patients With Chronic Hepatitis C Infection

Acetaminophen and Your Liver

DDW: Hepatitis Patients at Risk for Accidental Acetaminophen Toxicity

 (05/23/06)

Acetaminophen (Tylenol, Paracetamol) Overdose IS Easier Than Many Realize - (01/30/06)

Abstract T1045 – Impact Of Alcohol Dependence On The Health Values Of Patients Infected With HCV

 

   
   
   

Drug Interactions with "peginterferon alfa-2a"

The following drugs are known to interact with "peginterferon alfa-2a".

Please click on a drug name to check the interaction details.

A red icon denotes a possible severe interaction,

a blue icon denotes a possible moderate interaction,

and a green icon denotes a possible mild interaction.

 

 
Aerolate III Aerolate JR
Aerolate SR alemtuzumab
aminophylline Amipaque
anisindione Aquaphyllin
Asmalix Bronkodyl
Campath Choledyl
Choledyl SA Coumadin
Cytovene
dicumarol
Elixophyllin ganciclovir
Hycamtin metrizamide
Miradon Orap
oxtriphylline pimozide
Quibron-T Quibron-T/SR
Requip Respbid
ropinirole Slo-Bid Gyrocaps
Slo-Phyllin Slo-Phyllin 125
Slo-Phyllin 80 Theo-24
Theobid Theochron
Theoclear L.A.-130 Theoclear L.A.-260
Theoclear-80 Theo-Dur
Theo-Dur Sprinkles Theolair
Theolair-SR theophylline
Theosol-80
Theo-Time
Theovent Theo-X
topotecan T-Phyl
tramadol Truphylline
Truxophyllin Ultram
Uniphyl Uniphyl CR
Valcyte valganciclovir
warfarin Adriamycin PFS
Adriamycin RDF Chirocaine
cyclophosphamide Cytoxan
Cytoxan Lyophilized Doxil
doxorubicin doxorubicin liposomal
levobupivacaine Neosar
Rubex

 

   
 

The following drugs are known to interact with "ribavirin".

Please click on a drug name to check the interaction details.

A red icon denotes a possible severe interaction,

a blue icon denotes a possible moderate interaction,

and a green icon denotes a possible mild interaction.

 
abacavir anisindione
Coumadin dicumarol
didanosine Epivir
Epivir HBV Hivid
lamivudine Miradon
Retrovir stavudine
tenofovir Videx
Videx EC

 

   
 

Herbs with Drug Interactions - a Partial List

By popular request, here is a partial list of herbs with drug interactions.  It is by no means complete!  If you are taking medications, please check with your prescribing physician before taking any supplements.

 

Herb - alphabetical by common name Possible Drug Interaction Possible Contraindications
Ashwaganda Withania somnifera None known. (PPP, 601) May potentiate the effects of barbituates (Atal and Schwarting). (BSH, 124) High dosages of alkaloids from Withania exhibit prolonged hypotensive, bradycardiac and respiratory stimulant actions, may also have depressant effect on higher cerebral centres; sedative effects have also been demonstrated. (CAACH, 138)
Bilberry Vaccinium myrtillus None known. (HM, 18; TGHM, 88) Possible interaction with warfarin and antiplatelet drugs in very high doses. (PPP, 301)  Very high doses should be used cautiously in patients with haemorrhagic disorders and in those taking warfarin or antiplatelet drugs. (PPP, 301)
Bladderwrack Fucus vesiculosus None known. (HM, 213) Caution indicated within iodine-containing drugs. (AEHD, 44)  Therapeutic use is not recommended in hyperthyroidism, long-term therapeutic use is not recommended. (BSH, 54) Contraindicated in hyperthyroidism, cardiac problems. (BHC, 38) In rare cases allergic reactions involving serious overall reactions may occur. (TGHM, 315)
Black Cohosh Cimicifuga racemosa Drugs for iron therapy Inhibits iron absorption
Bugleweed Lycopus virginicus
 
 None known. (TGHM, 99) Do not take with thyroid medications. (BSH, TGHM, 99) Contraindicated in thyroid hypofunction, enlargement of the thyroid without functional disorders. (TGHM, 99; BSH, 72) Administration of the herb interferes with diagnostic procedures using radioactive isotopes. (TGHM, 99)
Bupleurum Bupleurum falcatum
 
The use of alcohol, sedatives and other central nervous system depressants, in conjunction with this herb, may cause synergistic sedative effects. (WHO, 73) Bupleurum has a slight sedative effect in some patients and may also increase bowel movements and flatulence (wind). (CAACH, 23; WHO, 73, 74; PPP, 317) May cause nausea and reflux in sensitive patients. (PPP, 317) 
Californian Poppy
Eschscholtzia californica
 May potentiate pharmaceutical MAO-inhibitors. (BSH, 49) This herb should be restricted in its application to experienced and well-trained practitioners. (PPP, 232) There is a theoretically increased risk of neurotoxicity and other adverse effects (although no known incidence). (PPP, 233) The following cases should be approached with caution: (1) concurrent prescription of powerful analgesics, (2) pain in children, (3) neurological disease, (4) depression and psychosis, (5) liver and kidney disease, and (6) history of allergic or anaphylactic reactions. (PPP, 232)
Cascara sagrada Rhamnus purshiana Most intestinally absorbed drugs; Thiazide-type diuretics Interferes with absorption of the pharmaceutical agent; Raise blood pressure or deplete potassium
Chamomile Matricaria recutita Drugs for iron therapy Inhibits iron absorption
Coleus Coleus forskohlii Forskolin has the ability to potentiate many drugs. Use cautiously in patients taking prescribed medication. (CAACH, 106) Contraindicated in hypotension. (CAACH, 106) 
Dong Quai Angelica sinensis  Based on animal studies, caution is advised for patients receiving chronic treatment with anticoagulant drugs such as Coumadin (warfarin). (PPP, 352) Containdicated in bleeding or very heavy menstruation, first trimester of pregnancy, acute viral infections such as colds or influenza. (CAACH, 5-6; BSH, 11; PPP, 352) Also contraindicated in diarrhea caused by weak digestion and in haemorrhagic disease. (PPP, 352) Cardiovascular side effects include excessive bleeding. (TCPHP, 290) Dong quai has two furanocoumarins (psoralen and bergapten), which are photoreactive and have the potential to cause severe photodermatitis. These furanocoumarins are also photocarcinogenic. However, the risk of phototoxicity in humans from ingestion of Dong quai has not been characterized. (TCPHP, 290-291) 
Echinacea Echinacea purpurea  None known. (HM, 97; TGHM, 123; WHO, 142; PPP, 360) Commission E cautioned that the herb should not be used in systemic diseases such as tuberculosis, leukosis, collagenosis, multiple sclerosis, AIDS, HIV infections, and other autoimmune diseases (based on theoretical considerations and not on any reports of adverse findings). (HM, 97; TGHM, 123; WHO, 141-142; PPP, 359) Caution is advised for transplant patients taking immunosuppressive drugs; short-term therapy is suggested. (PPP, 360) Should not be administered to patients with known allergy to any plant of Asteraceae (Compositae). (WHO, 142; PPP, 359; HM, 97) Allergic concern based upon case reports. (TCPHP, 301; PPP, 359; WHO, 142)
Evening Primrose Oil Oenothera biennis Anticonvulsants and tricyclic antidepressants Lowers the seizure threshold, thus increasing drug dosage requirements
Feverfew Tanacetum parthenium Drugs for iron therapy; Warfarin sodium, heparin, aspirin and other anticoagulants Inhibits iron absorption; Augments the anticoagulant effect, thus altering clotting or bleeding times
Garlic Allium sativum
 
Contains glucose. Use with caution in patients taking anti-platelet drugs. Garlic’s antiplatelet effect might be dangerous in patients taking warfarin or antiplatelet agents such as aspirin, ticlopidine, clopidogrel, or dipyrida-mole. (TCPHP, 118; HM, 115; WHO, 25)  Contraindication with gastrointestinal disturbance; in rare instances, there may be changes to the flora of the intestine, or allergic reactions. (TGHM, 134; HM, 145; BSH, 6; BHC,106) May also cause heartburn, nausea, vomiting, and diarrhea if taken on an empty stomach. (WHO, 26) HM suggests that substantial amounts of garlic should not be consumed prior to surgery. (HM, 145) May increase the risk of postoperative bleeding. (WHO, 25; ESCOPM, 2; AEHD, 229) Allergic and dermatologic concern based upon case reports. (AEHD, 229; WHO, 26; TCPHP, 116-117, 301) Hematologic concern based upon in vitro data and case reports. (TCPHP, 301) 
Ginger Zingiber officinale Contraindicated with gallstones; consult a physician first. (HM, 156; BSH, 125; TGHM, 136) May increase the chance of bleeding. (PPP, 401) Overdose may lead to a blood-thinning effect and an increase in gastric secretory activity leading to heartburn. (PPP, 401; ESCOPM, 1996, 1) Topical application may cause contact dermatitis in sensitive patients. (PPP, 401); Warfarin sodium, heparin, aspirin and other anticoagulants None known. (HM, 156, TGHM, 136) Caution should be used in patients taking anticoagulants and antiplatelet drugs because of its potential antiplatelet effect. (TCPHP, 129; CAACH, 106) May increase the absorption of pharmaceutical drugs. (PPP, 401) Caution indicated with patients taking blood-thinning drugs such as warfarin, or aspirin or who have increased risk of haemorrhage. (PPP, 401) May enhance absorption of sulphaguanidine. (ESCOPM, 1); Augments the anticoagulant effect, thus altering clotting or bleeding times
Ginko Ginko biloba Warfarin sodium, heparin, aspirin and other anticoagulants Augments the anticoagulant effect, thus altering clotting or bleeding times
Ginseng and other herbs that contain cardiac glycosides Insulin and related drugs for diabetes mellitus; Digoxin; Warfarin soldium, heparin, aspirin and other anticoagulants Affects glucose levels; compromises dosage potency; alters bleeding or clotting times
Golden Seal Hydrastis canadensis  Berberine, an alkaloid constituent of this herb, may reinforce the effects of other drugs which displace the protein binding of bilirubin. (PPP, 295) Contraindicated in hypertensive conditions. (PPP, 294) Fresh plant may cause irritation to the mucosa. (BSH, 62) Canadian regulations do not allow golden seal as a non-medicinal ingredient for oral use products. (BSH, 62)
Hawthorn Crataegus monogyna 
 
digitalis glycosides, beta-blockers and other hypotensive drugs  May potentate the actions of digitalis, though this action has not been confirmed. (HM, 186-188) Hawthorn may act in synergy with digitalis glycosides, beta-blockers and other hypotensive drugs. Modification of drug dosage may be required. (PPP, 446) Drug interactions are also theoretically possible with cardioactive medications. (TCPHP, 257)
Kava Kava Piper methysticum Potentiation of effectiveness is possible for substances on the central nervous system, such as alcohol, barbituates and psychopharmacological agents. (TGHM, 156; PPP, 462) Caution indicated with medications for insomnia or anxiety such as benzodiazepine. (PPP, 463; TCPHP, 33) There is a risk of sudden abnormal movements (a dystonic reaction) when combined with antipsychotic drugs. (TCPHP, 37) May reduce the efficacy of Levodopa, a medication for Parkinson’s disease; may interact with antiplatelet drugs or anticoagulants (e.g., warfarin, heparin) however there are no case reports of such interactions. (TCPHP, 36) Extended use can cause discoloration of the skin, nails, and hair. (TGHM, 156; PPP, 462) In rare cases, contact type dermatitis can occur. (PPP, 462) Also accommodative disturbances, such as enlargement of the pupils and disturbances of the oculomotor equilibrium, have been reported. (TGHM, 156; TCPHP, 35) Contraindicated in endogenous depression. (HM, 223) Chronic usage may result in skin rash, shortness of breath, liver damage and neurological manifestations may occur. (PPP, 463) dermatologic and neurologic concern based upon case reports. (TCPHP, 301) Do not exceed recommended dose. (BSH, 86) 
Korean Ginseng Panax ginseng  May interact with monoamine oxidase inhibitor phenelzine and also with warfarin. (PPP, 429; WHO, 176). Do not use with stimulants, including excessive use of caffeine. (HM, 174, PPP, 429) Contraindicated for hypertension. (BSH, 81; HM, 174) Contraindicated with signs of heat, acute infections, acute asthma, hypertension, excessive menstruation or nose bleeds. (PPP, 429; CAACH, 41) Consuming caffeine with ginseng increases the risk of overstimulation and gastro-intestinal upset. (BSH, 81; BHC, 116) Higher doses can over-stimulate and aggravate insomnia, irritability, depression, headache, palpitation, hypertension, and can cause tremor, euphoria, skin eruptions, menstrual abnormalities, diminished sexual function and weight loss. (BSH, 81; CAACH, 40). May reduce blood glucose levels, diabetic patients should consult with physician. (WHO, 176)
Licorice Glycyrrhiza glabra  Should not be taken concurrently with corticosteroid treatment. (WHO, 190; AEHD, 77) Concurrent use of furosemide may potentiate development of acute renal failure. (AEHD, 77) Potassium loss due to other drugs, e.g. thiazide diuretics, can be increased. With potassium loss, sensitivity to digitalis glycosides increases. (HM, 237; TGHM, 161; WHO, 190) Should not be administered in conjunction with spironolactone or amiloride. (WHO, 190) Insulin may be synergistic with glycyrrhizin in causing electrolyte disturbances and suppression of renin and aldosterone. (AEHD, 77) It is recommended that patients with cardiovascular or renal disease use licorice only under care of physician. (TCPHP, 232; PPP, 474) Patients prone to potassium deficiency are also advised not to use licorice. (TCPHP, 232; TGHM, 161) Treatment not to exceed six weeks. (TCPHP, 232; BSH, 58; TGHM, 162) Contraindications: cholestatic liver disorders, liver cirrhosis, hypertonia, hypokalemia, and severe kidney insufficiency. (HM, 236; BSH, 58; BHC,146; TGHM, 161; WHO, 190; AEHD, 72) Also contraindicated if there is edema or congestive heart failure. (PPP, 474) Ingestion of large amount can lead to severe hypertension, cardiac arrhythmias, cardiomyopathy, and cardiac arrest. (AEHD, 73; BSH, 58; BHC, 146; AEHD, 72) 
Marshmallow Althaea officinalis Absorption of other drugs taken simultaneously may be delayed. (BSH, 9; HM, 245, 247; ESCOPM, 1; TGHM, 166, 167) As a mucilage or respiratory demulcent, contraindicated or at least inappropriate in congestive bronchial, catarrhal and congestive conditions of the mucosa. (PPP, 169, 211) 
Oregon Grape Berberis aquifolium
 
Berberine, an alkaloid constituent of this herb, may potentiate other drugs which displace the protein binding of bilirubin. (PPP, 295) This herb is classified as a choleretic and cholagogue. It is either contraindicated or at least inappropriate in the following: (1) obstructed bile ducts, (2) unconjugated hyperbilirubinaemia, (3) acute or severe hepatocellular disease, (4) septic cholecystitis (where there is risk of peritonitis), (5) intestinal spasm or ileus, and (6) liver cancer. (PPP, 187) As an alterative, this herb may be provocative to skin disease, and care needs to be taken to reduce the prospects of exacerbations. (PPP, 254) 
Pau D'Arco Tabebuia avellanedae Patients on anticoagulant therapy should not be prescribed Pau D’Arco due to the warfarin-like action of naphthoquinones at high doses. (PPP, 504) Contraindicated with anticoagulants. (PPP, 504) Adverse effects are not expected when consumed with the recommended dosage. (PPP, 500)
St. John's Wort Hypericum perforatum  None known. (ESCOPM, 2; TGHM, 215; HM, 363) May potentiate pharmaceutical MAO-inhibitors. (BSH, 62, 173) Recommend physician consultation when taken with MAO inhibitors, SSRIs, and tricyclics. (PPP, 549); Drugs for iron therapy Contraindicated in the treatment of serious depression with psychotic symptoms, suicidal risk or signs and symptoms that are so severe that they do not allow the patient’s family or work involvements to continue. (PPP, 549) May cause mild stomach discomfort, skin rash, tiredness, fatigue, sleep disturbances, photosensitization is possible, especially in fair skinned individuals. (BSH, 62; TGHM, 215; HM, 363; PPP, 548; ESCOPM, 1996, 1) Caution advised in very severe debility, especially if associated with immune or digestive collapse, renal or hepatic failure, rampant cancer or strong regimes of chemotherapy. (PPP, 155) dermatologic and neurologic concern based upon case reports. (TCPHP, 301); Inhibits iron absorption
Sarsaparilla Smilax ornata Commission E advises of potential drug interactions with hypnotics, digitalis glycosides, and bismuth. However, no other reference substantiates these concerns. (BSH, 108) Risks: taking the herb may lead to gastric irritation and temporary kidney impairment [diuresis]. The absorption of simultaneously administered substances may be increased. The elimination of other substances (e.g., hypnotics) is accelerated. This can cause an uncontrolled condition of increased or decreased action of herbs taken simultaneously. (TGHM, 372)
Tribulus Tribulus terrestris  This herb may increase FSH in women, which in turn increases levels of oestrogen. (PPP, 46)  Due to the presence of saponins, this herb may be a gastrointestinal irritant. (PPP, 46)
Turmeric Curcuma longa
 
None known. (HM, 382; TGHM, 222) High doses should not be given to patients taking antiplatelet or anticoagulant drugs. (PPP, 578) Contraindicated in obstruction of bile passages; in case of gallstones, use only after consulting with a physician. (TGHM, 222; HM, 382; WHO, 121; PPP, 578) The herb should not be administered to patients who suffer from stomach ulcers or hyperacidity. (BSH, 39; HM, 382) Occasional cases of allergic dermatitis reported. (WHO, 121; PPP, 578) Patients applying topical doses should be cautioned against excessive exposure to sunlight. (PPP, 578) 
Valerian Valeriana officinalis  None known. (TGHM, 226; ESCOPM, 2; HM, 397) May increase the effects of CNS depressants or alcohol when taken together. (PPP, 587; AEHD, 172; WHO, 273) The herb may be expected to have at least an additive effect with barbiturates, alcohol, benzodiazepines, and other CNS depressants. (TCPHP, 64); diphenlydramine Can aggravate a sensation of tiredness or drowsiness, particularly in higher doses. (PPP, 587; WHO, 273) Overdose can result in blurred vision, erratic heart beat, headache, nausea, restlessness, visual illusions, even spasmodic movements. (PPP, 588; BSH, 120) Very large doses may cause bradycardia and arrhythmias, and decrease intestinal motility. (WHO, 274) Canada allows products containing valerian for use as sleeping aids and sedatives. (TCPHP, 64) Hepatic and neurologic concern based upon case reports, although in the case of alleged hepatotoxicity coingestants were involved. (TCPHP, 301)
Yohimbe Pausinystalia yohimbe Monoaminoxidase inhibitors Causes hypertension, insomnia, headache, and tremulousness

http://rainforesttreasure.com/drug_interact.asp

 
     

A western MD's view of the use of herbs by patients with HCV

 
EASL
39th Annual European Association for the Study of the Liver Conference
Berlin, Germany
April 14-18, 2004
 
 
 
 
Daily Cannabis Smoking as a Risk Factor for Fibrosis Progression in Chronic Hepatitis C
 
 
 
  A French research group reported results from this study at EASL (April 14-18, 2004, Berlin, Germany).
 
C. Hezode^{1}, F. Roudot-Thoraval ^{2}, P. Grenard ^{3}, B. Julien ^{3}, E.S. Zafrani ^{4}, D. Dhumeaux ^{1}, S. Lotersztajn ^{3}, A. Mallat ^{1} ^{3}; ^{1}Department of Hepatology, Hopital Henri Mondor, Creteil, France; ^{2}Department of Public Health, Hopital Henri Mondor, Creteil, France; ^{3}INSERM U581, Hopital Henri Mondor, Creteil, France; ^{4}Department of Pathology, Hopital Henri Mondor, Creteil, France
 
AUTHOR'S CONCLUSIONS: This study shows a strong link between daily cannabis consumption and fibrosis progression rate in patients with chronic hepatitisC. These results support experimental data demonstrating the profibrogenic role of CB1 receptors, see below (Grenart et al). Daily cannabis consumption should be avoided in patients with chronic hepatitis C. In multivariate analysis, fibrosis progression rate >0.08 U per year was independently related to a 4 times greater risk from daily cannabis smoking; alcohol intake _30 grams/day showed double the risk for faster fibrosis progression; age at contamination >24 years was associated with a 4 times greater risk for faster fibrosis progression; and activity _A2 was associated with 7 times greater risk for faster fibrosis progression. Pharmacologic antagonists of CB1 receptors may represent a new approach in the treatment of liver fibrosis.
 
Note from Jules Levin: Interestingly, Diana Sylvestre found in study that smoking marijuana increased sustained viral response rates of patients on Methadone Maintenance. The suggestion is that smoking pot may have improved adherence and tolerability of interferon/ribavirin therapy.
 
Several host, viral and environmental factors modulate development of fibrosis in patients with chronic hepatitis C. Progression may occurin the absence of risk factors.
 
Cannabis sativa, also known as marijuana, contains a predominant psychoactive cannabinoid, tetrahydrocannabinal (THC) and over 60 other cannabinoid compounds.
 
Biological effects of THC and other cannabinoids are mediated by 2 types of receptors CB1 and CB2.
 
Study authors said we recently demonstrated the profibrogenic role of CB1 receptors (P Grenard et al):
 
---CB1 receptors are highly upregulated in hepatic myofibroblasts of human cirrhotic liver samples
 
---following chronic tetrachloride administration, CB1 knock out mice showreduced fibrosis compared to wild type mice
 
The AIM OF THIS STUDY is to evaluate the impact of cannabis smoking on fibrosis progression rate in patients with chronic hepatitis C.
 
PATIENTS
--211 consecutive naïve patients with histologically proven chronic hepatitis C
--known disease duration
--no HBV or HIV coinfection
--no previous immunosuppression
 
METHODS
 
Epidemiological data:
--gender
--age at exposure, duration og HCV infection
 
Alcohol and tobacco consumption over the course of infection
 
Cannabis questionnaire:
--age at onset and duration of smoking
--amount and frequency of cannabis cigarettes
 
BMI and glucose fasting level
 
Genotype (INNO-LIPA HCV II, innogenetics)
 
Activity, fibrosis, and steatosis: METAVIR
 
ENDPOINTS
 
Fibrosis progression rate (fibrosis stage/duration of infection)
 
--rapid fibrosers: >0.08 U/yrs (median value
 
Significant fibrosis: ≥F2 (METAVIR)
 
CANNABIS CONSUMPTION
 
 
  Patients Cannabis cigarettes/month
Nonsmokers 108 (51%) 0
Occasional smokers 35 (17%) 7.2
Daily smokers 68 (32%) 107.6


 

 
 

  None Occasional Daily P
  N=108 n=35 n=68  
Male 57% 74% 91% <0.001
Age at exposure 28 21 21 <0.001
Disease duration 20 16 16 0.02
IVDU 16% 86% 93% <0.001
Genotype 3 13% 32% 43% <0.001
Tobacco(packs/yr) 8 16 6 <0.001
Alcohol (g/day) 13 43 38 <0.001
Glucose <6 mmol/L 89% 100% 94% 0.15
BMI (kg/m2) 25.4 23.3 23.4 0.009
Steatosis (moderate-marked) 32% 17% 32% 0.4
activity ≥A2 63% 60% 65% 0.9
fibrosis ≥F2 41% 23% 47% 0.06


 

 
FIBROSIS PROGRESSION RATE >0.08 U/year: Univariate analysis
 
AGE
Fibrosis Rate >0.08 U/yr
P=0.01
<=24 yrs: 41%
>24 yrs: 59%
 
ALCOHOL
Fibrosis Rate >0.08 U/yr
P=0.007
<30 grams/day: 42%
>30 grams/day: 62%
 
GENOTYPE
FibrosisRate >0.08 U/yr
P=0.005
Non 3: 42%
Genotype 3: 65%
 
GLUCOSE
Fibrosis Rate >0.08 U/yr
P=0.006
Glucose <=6: 46%
Glucose >6: 81%
 
STEATOSIS
Fibrosis Rate >0.08 U/yr
P=0.001
Absent/mild: 41%
Moderate/marked: 65%
 
ACTIVITY
Fibrosis rate >0.08 U/yr
P<0.001
A1: 22%
≥A2: 64%
 
CANNABIS
FIBROSIS RATE >0.08 U/yr
P=005
None: 41%
Occasional: 40%
Daily: 65%
 
MULTIVARIATE ANALYSIS
 
 

  OR CI95% P
Activity ≥ A2 7.1 3.4-15.0 <0.001
Age at exposure >24 yrs 4.8 2.1-10.9 <0.001
Genotype 3 3.1 1.3-7.0 0.01
Alcohol intake ≥30g/day 2.1 1.0-4.6 0.04
Daily cannabis 4.0 1.6-9.8 0.006


 

 
FIBROSIS STAGE and DAILY CANNABIS SMOKING ACCORDING TO AGE AT LIVER BIOPSY
 
If ≥ 40 yrs old: 58% of DAILY SMOKERS vs 44% of non & occasional smokers had Fibrosis ≥ F2.
 
If <40 yrs old: 23% of non and occasional smokers vs 43% of daily smokers had Fibrosis ≥ F2.
 
FIBROSIS STAGE and DAILY CANNABIS SMOKING ACCORDING TO AGE AT LIVER BIOPSY AND ALCOHOL INTAKE
 
DIFFERENCES SIGNIFICANT
If < 40 yrs old & alcohol <30 grams/day: 20% of non and occasional smokers vs 37% of daily smokers had Fibrosis ≥ F2.
 
If ≥ 40 yrs old & alcohol <30 grams/day: 35% of non and occasional smokers vs 71% of daily smokers had Fibrosis ≥ F2.
 
DIFFERENCES NOT SIGNIFICANT
If Alcohol >30 grams/day and < 40 yrs old: 38% of non and occasional smokers vs 50% of daily smokers had Fibrosis ≥ F2.
 
If Alcohol > 30 grams/day and > 40 yrs old: 76% of non and occasional smokers vs 50% of daily smokers had Fibrosis > F2.
 
 

 
 

www.natap.org


 

AASLD: Smoking Marijuana Raises Fibrosis Risk in Patients With Chronic Hepatitis C Infection

By Mark L. Fuerst

BOSTON, MA -- November 2, 2004 -- Daily marijuana smokers who have chronic hepatitis C infection risk having rapid progression of liver fibrosis, according to research presented here October 31st at the 55th Annual Meeting of the American Association of Liver Diseases.

Cannabis, the active ingredient in marijuana, exerts its biological effects through the binding of two receptors, CB1 and CB2. Ariane Mallat, Professor in the Hepatology and Gastroenterology Service at the Henri Mondor Hospital, Creteil, France, and colleagues previously demonstrated that CB1 receptors enhance fibrogenesis in mice, and set out to evaluate the clinical relevance of this finding in patients with chronic liver disease.

In 211 subjects with ongoing chronic hepatitis C infections, the researchers collected data on demographics, route of transmission, age at exposure, duration of hepatitis C virus infection, intakes of alcohol, tobacco, and cannabis over the course of the disease, maintenance treatment with methadone or buprenorphine, body mass index, fasting glucose level, genotype, steatosis, histological activity, and fibrosis level and progression.

Responses show that 32.2% of patients had used marijuana daily since the beginning of their disease (mean duration of 16 years), 16.6% were occasional smokers (once every other week), and 51.2% never smoked marijuana.

Univariate analysis showed that two-thirds of the daily smokers had a rapid rate of fibrosis progression compared to 40% of occasional smokers and 41% of non-smokers. In a multivariate analysis, a rapid fibrosis progression rate was related to daily cannabis use (odds ratio [OR] = 4.0), as was excessive daily alcohol intake (30 g; OR = 2.1), age at exposure of more than 24 years (OR = 4.8), and genotype 3 (OR = 3.1). There was no increased risk of progression among occasional smokers compared to non-smokers.

"In chronic hepatitis C infection, there is a strong relationship between daily cannabis use and fibrosis progression rate," Dr. Mallat said. "Patients with ongoing chronic hepatitis C should be advised against daily cannabis use, since regular use over the span of the disease is an aggravating factor regarding fibrosis progression."

This study supports the experimental data that demonstrated the profibrogenic role of CB1 receptors, she said, and noted that patients with chronic liver disease have a large amount of CB1 receptors in the liver, and that the impact of marijuana smoking is as a cofactor, and is not responsible for liver fibrosis per se.


[Presentation title: "Daily Cannabis Smoking as a Risk Factor for Fibrosis Progression in Chronic Hepatitis C." Abstract 67]
http://www.docguide.com/news/content.nsf/news/8525697700573E188

5256F40005204E7?OpenDocument&id=48DDE4A73E09A96985256888007

8C249&c=Hepa%2fBiliary%20Other&count=10
 


 

 

  Acetaminophen and  your liver

Acetaminophen and Your Liver
Liz Highleyman


The pain-reliever acetaminophen is one of the best-selling over-the-counter medications, used by 100 million people each year. It is sold under many brand names, including Tylenol, and is an ingredient in hundreds of combination medications, both over-the-counter (such as Excedrin, Midol, NyQuil, and Sudafed) and prescription (such as Vicodin).

Most people believe that acetaminophen is safe, but it can cause serious liver damage—and even acute liver failure—if it is taken in high enough doses. In fact, it is one of the leading causes of liver failure in the United States, accounting for more than 56,000 emergency room visits and 100 deaths each year. Unsafe At Any Dose?

Most people are only at risk for liver toxicity if they take more than the normal recommended amount of acetaminophen. Most cases of liver damage occur in people who have taken at least 10-15 grams—more than twice the recommended dose. Many of the emergency room visits and deaths linked to acetaminophen poisoning are due to accidental or intentional overdoses (for example, suicide attempts).

But some people are more susceptible to acetaminophen toxicity and can experience liver damage even at the recommended dose. A study by the U.S. Food and Drug Administration (FDA) showed that about 20% of people with acetaminophen-related liver toxicity had taken less than the recommended daily amount. For other people, a dangerous dose is not much higher than the recommended dose—that is, the “window” between a therapeutic dose and a toxic dose is smaller for acetaminophen than it is for many other drugs. Some experts also believe that taking acetaminophen for several days in a row may cause a dangerous build-up of the drug in the body.

Acetaminophen is more likely to cause liver toxicity at near-normal doses when used by people who drink alcohol. In fact, people who drink regularly may be more prone to liver damage even if they do not consume alcohol and acetaminophen at the same time. There appears to be added risk even if people take acetaminophen a few hours, or in some cases longer, before or after drinking. Since the mid-1990s, the Tylenol package has included a warning against drinking alcohol when using the drug.

How Acetaminophen Harms the Liver
Like many drugs, acetaminophen is metabolized by the liver. If the normal processing pathway is overwhelmed by a high dose, a different pathway known as the cytochrome P450 enzyme system kicks in. When this happens, a toxic metabolic byproduct called NAPQI is produced that can kill liver cells. Alcohol and many other drugs also use the cytochrome P450 processing system, and the risk of a “bottleneck” is greater if the liver has to deal with both acetaminophen and these other substances at the same time.

Acetaminophen poisoning has three stages. During the first 12-24 hours after taking the drug, a person may experience nausea and vomiting. During the second phase, from 24-48 hours, the person usually feels better. After 48-72 hours, however, liver enzyme (ALT and AST) levels start to rise, indicating liver injury. In the most severe cases, a person may develop acid buildup in the blood, excessive bleeding, and coma. At this stage, only a liver transplant can prevent death.

Fortunately, there is an antidote for acetaminophen poisoning. NAPQI is normally detoxified by a naturally occurring antioxidant called glutathione. But if too much acetaminophen is present, the body’s supply of glutathione can be used up. An amino acid called N-acetylcysteine (NAC), which restores glutathione in the cells, can be administered to reverse acetaminophen toxicity. NAC is most effective when used within 16 hours after taking acetaminophen; however, people often do not recognize that gastrointestinal symptoms could be an early sign of acetaminophen poisoning.

Fair Warning?
An FDA advisory panel recommended several times (most recently in September 2002) that products containing acetaminophen should carry a warning on the label about the risk of liver toxicity. In January 2004, the FDA launched a new public education campaign warning consumers about the potential risks of acetaminophen and other pain-relievers. Some companies now clearly label their products containing acetaminophen. This is important because unintentional overdoses can occur when people take two or more medications together without realizing they all contain acetaminophen. However, the FDA still does not require that such products carry a warning label concerning liver toxicity.

Acetaminophen for People with Hepatitis
What does all this mean for people with chronic hepatitis B or C? Doctors often recommend acetaminophen to relieve symptoms such as body aches and fever, which are common side effects of interferon therapy. For most people, acetaminophen is safe and effective. According to the FDA’s Dr. John Senior, “It’s very clear the average dose for the average person is very safe. But we are not all average people.” For many individuals, acetaminophen is still a good choice, especially considering that other over-the-counter pain-relievers can cause problems of their own (such as stomach bleeding with aspirin and nonsteroidal anti-inflammatory drugs).

The following tips can help prevent acetaminophen-related liver toxicity:

• Do not take more than the recommended dose of 4 grams within a 24-hour period (for example, 12 regular strength or 8 extra strength Tylenol tablets)
• Do not take the full day’s dose at one time; space it out over the course of the day
• Do not take acetaminophen for more than 10 days in a row
• Avoid drinking alcohol; this is important for people with hepatitis whether or not they use acetaminophen
• People who do consume 2-3 alcoholic drinks per day should not take more than half the usual recommended dose of acetaminophen (2 grams within 24 hours)
• People with advanced liver fibrosis or cirrhosis should avoid acetaminophen
• Write down how much acetaminophen you take, and when, if you have trouble remembering
• Check the labels of all medications; small doses of acetaminophen in combination remedies can add up to big trouble.

http://www.hcvadvocate.org/news/newsLetter/2005/advocate0105.html#3

 

 

   
 
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Reviewed June 05 2006