Case Reports in Medicine

Case Reports in Medicine / 2009 / Article

Case Report | Open Access

Volume 2009 |Article ID 918156 |

Grace Guzman, Eric R. Kallwitz, Christina Wojewoda, Rohini Chennuri, Jamie Berkes, Thomas J. Layden, Scott J. Cotler, "Liver Injury with Features Mimicking Autoimmune Hepatitis following the Use of Black Cohosh", Case Reports in Medicine, vol. 2009, Article ID 918156, 8 pages, 2009.

Liver Injury with Features Mimicking Autoimmune Hepatitis following the Use of Black Cohosh

Academic Editor: Anne M. Larson
Received21 Jul 2009
Accepted11 Nov 2009
Published10 Jan 2010


There are a growing number of cases detailing acute hepatic necrosis in patients taking black cohosh (Cimicifuga racemosa), an over-the-counter herbal supplement for management of menopausal symptoms. Our aim is to illustrate two cases of liver injury following the use of black cohosh characterized by histopathological features mimicking autoimmune hepatitis. Both patients reported black cohosh use for at least six months and had no evidence of another cause of liver disease. Their liver biopsies showed a component of centrilobular necrosis consistent with severe drug-induced liver injury. In addition, the biopsies showed characteristics of autoimmune-like liver injury with an interface hepatitis dominated by plasma cells. Although serum markers for autoimmune hepatitis were not particularly elevated, both patients responded to corticosteroids, supporting an immune-mediated component to the liver injury. Liver injury following the use of black cohosh should be included in the list of differential diagnoses for chronic hepatitis with features mimicking autoimmune hepatitis.

1. Introduction

Black cohosh (Cimicifuga racemosa) is an herbal supplement that is sold over-the-counter for management of menopausal symptoms, menstrual irregularities, and arthritis. There are now a number of manuscripts indicating liver injury from black cohosh [17]. Here, we present two patients who developed a drug-induced liver injury following the use of black cohosh characterized by centrilobular necrosis and histologic features mimicking autoimmune hepatitis (AIH) who improved with corticosteroid therapy.

2. Case Studies

The case series was approved by the Institutional Review Board at the University of Illinois at Chicago.

Case 1. A 42-year-old woman presented to her primary care provider with a two-month history of progressive malaise, nausea, vomiting, and dizziness. On physical examination, she had mild icterus and no stigmata of chronic liver disease. Her only comorbidity was hypothyroidism. Her medications included black cohosh, which she was taking for 6 months, and levothyroxine 0.05 mg daily. She discontinued black cohosh when her symptoms began. She had no family history of liver or autoimmune disease. She denied any alcohol or drug use. Her total bilirubin level was 3.1 mg/dL (normal 0.8–1.2), alanine transaminase (ALT) 1457 U/L (normal 5–40), aspartate transaminase (AST) 696 U/L (normal 10–40), alkaline phosphatase (ALP) 94 U/L (normal 30–120 U/L), and international normalized ratio (INR) 1.2 (normal 0.8–1.2). Further laboratories showed no serological evidence of active hepatitis A, B, or C infection. Serological titers for acute cytomegalovirus (CMV) and Epstein Barr virus (EBV) were negative. Antinuclear antibody (ANA) was 1 : 40 and smooth muscle antibody was modestly elevated at 1 : 80. Serum iron was 169  g/dL (normal: 50 to 170  g/dL for women), ferritin was 642 ng/dL (normal: 15–200 ng/mL for females), and hemochromatosis gene analysis was negative. Ceruloplasmin was in the normal range.
Four months after her initial presentation, the liver enzymes remained elevated with an ALT of 334 U/L, AST 229 U/L, and a total bilirubin of 1.4 mg/dL. A liver biopsy was performed which prompted a referral to the liver center at the University of Illinois. The liver biopsy was remarkable for necrosis around terminal hepatic venules, lobular disarray, mild ballooning, apoptosis, Kupffer cell reactivity, mild cholangiolar proliferation, and interface hepatitis remarkable for numerous plasma cells and eosinophils. A repeat antismooth muscle antibody was normal at 1 : 20. Prednisone treatment was initiated. A follow-up liver biopsy was performed after three months. At this time, the liver histology demonstrated chronic hepatitis with fibroinflammatory expansion of portal tracts by moderate plasma cell rich interface hepatitis, rare periportal hepatocyte apoptosis, and mild cholangiolar proliferation (Figures 1(a) and 1(b)). The patient was started on azathioprine. Her liver enzymes returned to normal values within five months with an ALT of 30 U/L, AST of 29 U/L, ALP 36 U/L, and a total bilirubin of 0.9 mg/dL. A repeat liver biopsy after fifteen months showed marked improvement with only minimal portal lymphocytes and no other significant histopathological changes. The liver function test values remained normal at 15 months and at 40 months following the acute episode. The clinicopathological features of Case 1 are illustrated in Tables 1, 2, and 3.

Clinical featuresCase 1Case 2

Age (years)4253
SignsMild icterusIncreased LFTs
SymptomsProgressive malaise, nauseaRUQ** abdominal pain, fatigue
Vomiting, dizzinessLower extremity edema
Stigmata of CLDAbsentAbsent

MedicationsBlack cohoshOTC with soy and black cohosh

IndicationMenopausal symptomsMenopausal symptoms
DoseNot specifiedNot specified
Duration6 months8 months

Other medicationsLevothyroxineDicyclomine; NSAID

IndicationHyperthyroidismGI cramps; pain
Dose0.05 mg dailyNot specified
DurationChronicAs needed

LFTs: Liver function tests.
RUQ: Right upper quadrant.
CLD: Chronic liver disease.
OTC: Over the counter drug.
NSAID: Nonsteroidal anti-inflammatory drug.

Case 1Case 2

Past medical historyViral or non-viral hepatitisAbsentAbsent
Alcohol consumptionAbsentAbsent

Serological testsAnti-HAV IgMAbsentAbsent
Anti-HAV totalAbsentAbsent
HBV surface antigenAbsentAbsent
Anti-HBV coreAbsentAbsent
Anti-HBV surfaceAbsentAbsent
EBV Ca IgMAbsentAbsent
EBV Ca IgGAbsentAbsent
EBV Na IgGAbsentAbsent
EBV IgGAbsentAbsent
Anti-CMV IgMAbsentAbsent

HCV RNA PCRNegativeNegative

Other laboratory valuesIron (normal: 50–70 μg/dL for women)169 μg/dL137 μg/dL
Ferritin (normal: 15–200 ng/mL in women)642 ng/mL1527 ng/mL
HFE gene analysisNegativeNegative

Case 1

Time of use to illness: 6 mo**

Time of use to discontinuation: 6 mo**

Time of presentation to the liver clinic**

Duration of illness in months247121540

Liver function tests (normal)
 Total bilirubin (0.8–1.2 mg/dL)
 ALT (5–40 U/L)1457334321303937
 AST (10–40 U/L)696229236293733
 ALP (30–120 U/L)946866363837
INR (0.8–1.2)

Autoimmune antibodies
 Antinuclear antibody1 : 401 : 20
 Antismooth muscle antibody1 : 80
Liver biopsy findings Acute hepatitisChronic hepatitisBiopsy at 15 mo.

 NecrosisCentral & portalAbsent
 InfiltratesMixed with eosinophilsPlasmacyticAbsent
 Other findingsDisarray, ballooning ApoptosisNo significant abnormality

Portal and periportal
 Cholangiolar proliferationModerateModerateAbsent
 Infiltrate severityModerateModerateMinimal
 Infiltrate predominant typeMixed with eosinophilsPlasmacyticLymphocytes
Fibrosis FibronecrosisFibronecrosisAbsent

Case 2. A 53-years-old woman presented to our liver center for evaluation of elevated liver enzymes detected at a health screening fair four months earlier. She had no risk factors for viral hepatitis, no family history of liver disease, and denied any alcohol consumption. Although she was initially asymptomatic, she developed right upper quadrant abdominal pain, fatigue, and lower extremity edema by the time of her presentation. Her medical history was remarkable only for irritable bowel syndrome. Her medications within the past year included dicyclomine for abdominal cramps as needed, an herbal supplement which contains soy protein and black cohosh for menopausal symptoms, and occasional over the counter nonsteroidal anti-inflammatory drugs (NSAIDs) for pain. She discontinued these medications on the advice of her primary care physician. Laboratories showed a total bilirubin of 2.0 mg/dL, ALT 443 U/L, AST 478 U/L, ALP 188 U/L, and an INR of 2.0. Other notable laboratory values included negative serological evidence of active hepatitis A, B, and C viral infection, undetectable hepatitis C virus RNA by PCR, iron 137  g/dL, ferritin 1527 ng/mL, negative hemochromatosis gene analysis, and nonsignificant ceruloplasmin level. Serological tests for antinuclear, antismooth muscle, antiliver kidney microsomal, and antimitochondrial antibodies were negative. An ultrasound demonstrated patent portal and hepatic veins and a normal appearing liver. Her liver biopsy was remarkable for centrilobular necrosis with moderate cholangiolar proliferation and plasma cell rich interface and lobular hepatitis.
The patient was started on 40 mg of prednisone daily. Liver function test values improved to a total bilirubin of 1.4 mg/dL, ALT of 60 U/L, AST 50 U/L, and ALP 153 U/L after two weeks and normalized after five weeks of therapy. The clinicopathological features of Case 2 are illustrated in Tables 1, 2, and 4.

Case 2

Time of use to illness: 8 months**

Time of use to discontinuation: 8 months**

Time of presentation to liver clinic**

Duration in months44.55


Liver function tests (normal values)
 Total bilirubin (0.8–1.2 mg/dL)
 ALT (5–40 U/L)4436030
 AST (10–40 U/L)4785038
 ALP (30–120 U/L)18815398
INR (0.8–1.2)2.01.3

Autoimmune antibodies
 Anti-nuclear antibodyNegative1 : 20
 Anti-smooth muscle antibodyNegative
Liver biopsy findings

 Other findingsDisarray, apoptosis

Portal and periportal
 Cholangiolar proliferationModerate
 Infiltrate severityModerate
 Infiltrate predominant typePlasmacytic
Fibrosis Fibronecrosis

3. Application of the Naranjo Causality Score for Adverse Drug Reactions

The Naranjo causality score for adverse drug reactions [8] was applied to the cases described here. As shown in Table 5, the current case studies individually achieved a Naranjo score of 3 and were both categorized as “possible adverse drug reaction”, in a scale encompassing a minimum score of zero, or “doubtful adverse drug reaction” to a maximum score of 9, or “definite adverse drug reaction.”

Question/Scoring-Yes/No/Do not know or unavailableCase 1Case 2

1Are there previous conclusive reports on this reaction? 1/0/000
2Did the adverse event appear after the suspected drug was given? 2/-1/022
3Did the adverse reaction improve when the drug was discontinued or a specific antagonist was given? 1/0/011
4Did the adverse reaction appear when the drug was readministered? 2/-1/000
5Are there alternative causes that could have caused the reaction? -1/2/0-1-1
6Did the reaction reappear when a placebo was given? -1/1/000
7Was the drug detected in any body fluid in toxic concentrations? 1/0/000
8Was the reaction more severe when the dose was increased/ increasing, or less severe when the dose was decreased? 1/0/011
9Did the patient have a similar reaction to the same or similar drugs in any previous exposure? 1/0/000

      Total score33

Scoring: >9 : definite adverse drug reaction (ADR).
5–8 : probable ADR.
1–4 : possible ADR.
0 : doubtful ADR.

4. Application of the Hennes-Simplified Criteria for Diagnosis of Autoimmune Hepatitis (AIH)

While the current case studies showed histopathological features of autoimmune hepatitis, neither fulfilled a diagnosis of “probable AIH” or “definite AIH” based on the Hennes simplified criteria for diagnosis of AIH [10]. Briefly, Case 1 had an ANA titer of up to 1 : 80 (score 2), no available immunoglobulin titers (no score), a liver histology compatible with AIH (score 1), and absence of viral hepatitis (score 2), with a total score of 5. Case 2 had a score of 1-0-1-2 4, on a scale where a score of 6 was designated “probable AIH”, and 7 as “definite AIH.”

5. Discussion

Botanical dietary supplements are used commonly in the United States and are generally perceived to be safe [11]. In one study, nearly one half of persons reported use of at least one agent to their primary provider [12]. A major difficulty in studying black cohosh is uncertainty regarding the composition of the various black cohosh products. Black cohosh itself contains a number of secondary compounds including phenolic derivatives and triterpene glycosides [13]. Phytoestrogens were postulated to play a role in black cohosh binding to estrogen receptors, but the presence of these compounds is controversial. In one study, chromatographic analysis of 11 commercial black cohosh products showed that three were actually Asian Actea species [13]. An analysis of the remaining eight products found variability in the composition of triterpene glycosides and phenolic constituents. More importantly, not a single product contained a phytoestrogen. Thus, the mechanism by which black cohosh might impact on alleviating menopausal symptoms is not well understood. Other possibilities include binding to yet-to-be-defined receptors or effects on the central nervous system [14]. Whether black cohosh is effective in controlling vasomotor symptoms of menopause is controversial as well. The American College of Obstetrics and Gynecology included black cohosh as a possible remedy for the vasomotor symptoms of menopause [15]. A large randomized-blinded trial of one-year duration found no difference between black cohosh and placebo in controlling vasomotor symptoms [16]. Moreover, a recent review did not recommend long-term use due to the absence of safety evaluation [17].

There are a growing number of case reports of hepatotoxicity in patients taking black cohosh (Table 6) [17]. Most described acute hepatic necrosis, although three articles of them detailed a case with clinical features of autoimmune hepatitis after black cohosh use [1, 2, 5]. The clinicopathological features of the cases in the current series have a fascinating combination of findings. Both patients presented with an acute hepatitis displaying prominent centrilobular necrosis consistent with severe drug-induced liver injury. While autoantibodies were low titer or absent, the histology showed characteristics of autoimmune hepatitis with a plasma cell rich interface and lobular hepatitis. In addition, both patients responded to corticosteroids, supporting an immune mediated component to the liver injury.

Case reportsWhiting Case 1*Whiting Case 2*Lontos*Levitsky*Cohen*Lynch*ChowNisbetCurrent study Case 1##  Current study Case 2


Botanical dietary contentsBlack cohoshBlack cohosh, skullcap#, Valerean, PassionflowerBlack cohosh, ground ivy#, golden seal, Gingko, oat seedBlack cohoshBlack cohoshBlack cohoshBlack cohoshBlack cohoshBlack cohoshBlack cohosh, soy

Other drugs LevothyroxineLevothyroxineLevothyroxineDicyclomine

Serologies indicating presence of other liver diseasesAbsentAbsentAbsentAbsentAbsent

Lab data indicating presence of other liver diseasesAbsentAbsentAbsentAbsentAbsent

Presenting symptomJaundiceALFALFALFJaundiceAcute hepatitisAcute hepatitisRUQ pain

Main liver biopsy findingAcute hepatitisAcute hepatitisMassive liver necrosisCentrilobular necrosisCentrilobular necrosis

Lobular infiltrateMixed + plasma cellsMononuclear infiltratePlasma cytic infiltrateLymphop-lasmacytic infiltrate
Other lobular findingsNecrosisBridging necrosisPreserved bile ducts, collapsed parenchymaLobular disarray Lobular disarray

TherapyPrednisoneImmuno-therapyPrednisonePrednisone & azathioprinePrednisone

InterventionOLTOLTOLTOLTWithdrawal of black cohoshWithdrawal of black cohoshWithdrawal of black cohosh

OutcomeRecoveryLF s/p d/c black cohoshRecoveryRecoveryLF death hemorrhageRecoveryRecoveryRecoveryRecovery
AIH like histologyPresentPresentPresentPresentPresent

Serological marker for AIHAbsent AbsentAbsentAbsentAbsentAbsent

Issues disputing validity of black cohosh hepatoxicityDrug use for only 6 daysMulti-drug productMulti-drug productMulti drug use Ethanol, NSAID & cyclovir7 day use; maybe AIH2 weeks exposure; cholelithiasisMaybe AIH

*Cases adapted from Table 1 Lynch [5]; ALF: Acute liver failure; RUQ: Right upper quadrant pain.
OLT: Orthotopic liver transplant; LF: Liver failure.
#Herbal remedies known as hepatotoxic; ##Also reported by Mahady [9]; AIH: Autoimmune hepatitis.

Determining the risk of black cohosh hepatotoxicity is further complicated by variability in both dosage and number of other botanical herbal supplements contained in some preparations. As an example, in the case reported by Lontos [4], the preparation of black cohosh included 4 other botanicals: ground ivy, golden seal, gingko, and oat seeds. While liver injury remains unreported with the use of the last 3 botanicals, ground ivy contains a known hepatotoxin, pulegone. This case culminated in liver failure despite discontinuation of the herbal supplement [4].

Drug interactions might further potentiate negative outcomes resulting from hepatoxicity due to herbal supplements. That subjects in 3 of 5 reported cases of autoimmune-like liver injury following consumption of black cohosh (Table 6) also had concomitant intake of synthetic thyroid hormone, levothyroxine, merits attention [2, 5]. Herbal supplements such as venencapsan and black cohosh, and prescription drugs specifically rosiglitazone, ritonavir, and valproic acid, have had reported drug interactions with levothyroxine [1, 9, 1822].

A 2008 review by Mahady assigned all known case reports of black cohosh-induced liver injury under the category of “possible causality” [9]. As earlier stated, both cases of the current study were also assigned “possible causality” by Naranjo scale [8]. Although no clinical or animal pharmacokinetic or toxicological information were identified in the Mahady review, it led to the inclusion of a cautionary statement on black cohosh products which was not previously required [9]. Despite such development, the use of botanical dietary supplements is generally viewed by the public as safe [11]. Providers are encouraged to screen patients about their consumption of botanical herbal supplements and to assess for any evidence of liver injury [1]. Timely discontinuation of hepatotoxic agents and, in some cases, early initiation of immunotherapy might prevent significant liver injury or could even be life saving [4].

The validity of reported cases of liver injury due to black cohosh illustrated in Table 6 has been disputed. Concerns that led to this uncertainty included cases in which the timing of liver injury occurred at a relatively short interval following exposure to black cohosh [2, 6, 7], presence of comorbidities such as cholelithhiasis [6] or concomittant use of drugs other than black cohosh that could have potentially triggered the adverse drug reaction [3, 4, 7], or the notion that some of the reported cases [2], including Case 1 of the current study (also reported by Mahady [23]), were indeed examples of autoimmune hepatitis rather than adverse drug reactions. Nonetheless, application of the Naranjo causality score to these case reports found possible cause for adverse drug reaction [8]. Further, autoimmune hepatitis is one of the known outcomes of drug-induced liver injury. The immune mechanism is precipitated by a drug or a metabolite acting as a hapten covalently binding to host cellular protein, converting into an immunogen [24] and thereby eliciting an autoimmune response. Outcomes illustrating an association of chronic hepatitis with autoimmune features developing following the use of the botanical supplement black cohosh need to be emphasized.

6. Conclusion

Here we described two cases of liver injury following the use of black cohosh characterized by chronic hepatitis with centrilobular necrosis and an interface activity dominated by plasma cells. While the histopathology in both cases was compatible with autoimmune hepatitis, clinical evidence for an autoimmune etiology was lacking. Nonetheless both cases improved upon withdrawal of the drug and immunosuppressive therapy, indicating that there was at least in part a drug-induced immunological basis to the liver injury.

The current case studies, and three other published cases of liver injury following the use of black cohosh, share similar histological characteristics [1, 2, 5]. Hepatic manifestations following the use of black cohosh should therefore be added to the list of differential diagnoses of hepatic necrosis culminating in chronic hepatitis mimicking autoimmune hepatitis.


  1. E. C. Chow, M. Teo, J. A. Ring et al., “Liver failure associated with the use of black cohosh for menopausal symptoms,” Medical Journal of Australia, vol. 188, no. 7, pp. 420–422, 2008. View at: Google Scholar
  2. S. M. Cohen, A. M. O'Connor, J. Hart et al., “Autoimmune hepatitis associated with the use of black cohosh: a case study,” Menopause, vol. 11, no. 5, pp. 575–577, 2004. View at: Publisher Site | Google Scholar
  3. J. Levitsky, T. A. Alli, J. Wisecarver et al., “Fulminant liver failure associated with the use of black cohosh,” Digestive Diseases and Sciences, vol. 50, no. 3, pp. 538–539, 2005. View at: Publisher Site | Google Scholar
  4. S. Lontos, R. M. Jones, P. W. Angus et al., “Acute liver failure associated with the use of herbal preparations containing black cohosh,” Medical Journal of Australia, vol. 179, no. 7, pp. 390–391, 2003. View at: Google Scholar
  5. C. R. Lynch, M. E. Folkers, and W. R. Hutson, “Fulminant hepatic failure associated with the use of black cohosh: a case report,” Liver Transplantation, vol. 12, no. 6, pp. 989–992, 2006. View at: Publisher Site | Google Scholar
  6. B. C. Nisbet and R. E. O'Connor, “Black cohosh-induced hepatitis,” Delaware Medical Journal, vol. 79, no. 11, pp. 441–444, 2007. View at: Google Scholar
  7. P. W. Whiting, A. Clouston, and P. Kerlin, “Black cohosh and other herbal remedies associated with acute hepatitis,” Medical Journal of Australia, vol. 177, no. 8, pp. 440–443, 2002. View at: Google Scholar
  8. C. A. Naranjo, U. Busto, E. M. Sellers et al., “A method for estimating the probability of adverse drug reactions,” Clinical Pharmacology and Therapeutics, vol. 30, no. 2, pp. 239–245, 1981. View at: Google Scholar
  9. G. B. Mahady, T. L. Dog, M. L. Barrett et al., “United States Pharmacopeia review of the black cohosh case reports of hepatotoxicity,” Menopause, vol. 15, no. 4, pp. 628–638, 2008. View at: Publisher Site | Google Scholar
  10. E. M. Hennes, M. Zeniya, A. J. Czaja et al., “Simplified criteria for the diagnosis of autoimmune hepatitis,” Hepatology, vol. 48, no. 1, pp. 169–176, 2008. View at: Publisher Site | Google Scholar
  11. J. D. Lewis and B. L. Strom, “Balancing safety of dietary supplements with the free market,” Annals of Internal Medicine, vol. 136, no. 8, pp. 616–618, 2002. View at: Google Scholar
  12. D. M. Eisenberg, R. B. Davis, S. L. Ettner et al., “Trends in alternative medicine use in the United States, 1990–1997: results of a follow-up national survey,” Journal of the American Medical Association, vol. 280, no. 18, pp. 1569–1575, 1998. View at: Google Scholar
  13. B. Jiang, F. Kronenberg, P. Nuntanakorn et al., “Evaluation of the botanical authenticity and phytochemical profile of black cohosh products by high-performance liquid chromatography with selected ion monitoring liquid chromatography-mass spectrometry,” Journal of Agricultural and Food Chemistry, vol. 54, no. 9, pp. 3242–3253, 2006. View at: Publisher Site | Google Scholar
  14. V. Viereck, G. Emons, and W. Wuttke, “Black cohosh: just another phytoestrogen?” Trends in Endocrinology and Metabolism, vol. 16, pp. 214–221, 2005. View at: Google Scholar
  15. ACOG Practice Bulletin, “Clinical management guidelines for obstetrician-gynecologists. Use of botanicals for management of menopausal symptoms,” Obstetrics and Gynecology, vol. 97, no. 6, supplement, pp. 1–11, 2001. View at: Google Scholar
  16. K. M. Newton, S. D. Reed, A. Z. LaCroix et al., “Treatment of vasomotor symptoms of menopause with black cohosh, multibotanicals, soy, hormone therapy, or placebo: a randomized trial,” Annals of Internal Medicine, vol. 145, no. 12, pp. 869–879, 2006. View at: Google Scholar
  17. F. Kronenberg and A. Fugh-Berman, “Complementary and alternative medicine for menopausal symptoms: a review of randomized, controlled trials,” Annals of Internal Medicine, vol. 137, no. 10, pp. 805–813, 2002. View at: Google Scholar
  18. P. A. De Smet, A. J. Van den Eertwegh, W. Lesterhuis et al., “Hepatotoxicity associated with herbal tablets,” British Medical Journal, vol. 313, no. 7049, p. 92, 1996. View at: Google Scholar
  19. H. E. Gouda, A. Khan, J. Schwartz et al., “Liver failure in a patient treated with long-term rosiglitazone therapy,” American Journal of Medicine, vol. 111, no. 7, pp. 584–585, 2001. View at: Publisher Site | Google Scholar
  20. N. L. Sheehan, M. J. Brouillette, M. S. Delisle et al., “Possible interaction between lopinavir/ritonavir and valproic acid exacerbates bipolar disorder,” The Annals of Pharmacotherapy, vol. 40, pp. 147–150, 2006. View at: Google Scholar
  21. M. Touzot, C. Le Beller, F. Touzot et al., “Dramatic interaction between levothyroxine and lopinavir/ritonavir in a HIV-infected patient,” AIDS, vol. 20, no. 8, pp. 1210–1212, 2006. View at: Publisher Site | Google Scholar
  22. A. Tseng and D. Fletcher, “Interaction between ritonavir and levothyroxine,” AIDS, vol. 12, no. 16, pp. 2235–2236, 1998. View at: Google Scholar
  23. G. B. Mahady, D. Fabricant, L. R. Chadwick et al., “Black cohosh: an alternative therapy for menopause?” Nutrition in Clinical Care, vol. 5, pp. 283–289, 2002. View at: Google Scholar
  24. W. Bleibel, S. Kim, K. D'Silva, and E. R. Lemmer, “Drug-induced liver injury: review article,” Digestive Diseases and Sciences, vol. 52, no. 10, pp. 2463–2471, 2007. View at: Publisher Site | Google Scholar

Copyright © 2009 Grace Guzman et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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