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Lamisil (Terbinafine) - Hepatic Function Abnormal - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Hepatic Function Abnormal (10)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Lamisil (Terbinafine) where reactions include hepatic function abnormal. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Lamisil side effects in 28 year old male

Reported by a pharmacist from Ireland on 2012-03-15

Patient: 28 year old male

Reactions: Myalgia, Hepatic Function Abnormal, Arthralgia, Liver Function Test Abnormal, Flank Pain, Medial Tibial Stress Syndrome, Mobility Decreased

Drug(s) suspected as cause:
Lamisil



Possible Lamisil side effects in female

Reported by a pharmacist from Japan on 2012-03-05

Patient: female, weighing 50.0 kg (110.0 pounds)

Reactions: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Hepatic Function Abnormal, Alanine Aminotransferase Increased, Dyspnoea Exertional, Malaise, Interstitial Lung Disease, Aspartate Aminotransferase Increased, Decreased Appetite

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Lamisil

Other drugs received by patient: Solu-Medrol; Prednisolone; Olopatadine HCL; Prednisolone; Prednisolone



Possible Lamisil side effects in female

Reported by a pharmacist from Japan on 2012-02-17

Patient: female, weighing 50.0 kg (110.0 pounds)

Reactions: Malaise, Dyspnoea Exertional, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Hepatic Function Abnormal, Interstitial Lung Disease, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Decreased Appetite

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Lamisil

Other drugs received by patient: Prednisolone; Prednisolone; Olopatadine HCL; Prednisolone; Solu-Medrol



Possible Lamisil side effects in 65 year old female

Reported by a pharmacist from Japan on 2012-02-06

Patient: 65 year old female

Reactions: Hepatic Function Abnormal, Dyspnoea, Blood Creatine Phosphokinase Increased, Interstitial Lung Disease, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Decreased Appetite

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Lamisil
    Dosage: 125 mg, qd
    Administration route: Oral
    Indication: Tinea Infection
    Start date: 2011-11-09
    End date: 2011-11-24

Olopatadine HCL
    Dosage: 5 mg, qd
    Administration route: Oral
    Start date: 2011-11-09
    End date: 2011-11-24

Other drugs received by patient: Prednisolone; Solu-Medrol; Prednisolone; Prednisolone



Possible Lamisil side effects in 60 year old female

Reported by a physician from Japan on 2012-02-06

Patient: 60 year old female

Reactions: Hepatic Function Abnormal, Hypoglycaemia

Drug(s) suspected as cause:
Glyburide
    Administration route: Oral
    Indication: Type 2 Diabetes Mellitus
    End date: 2011-12-01

Januvia
    Administration route: Oral
    Indication: Type 2 Diabetes Mellitus
    End date: 2011-12-01

Lamisil
    Administration route: Oral
    Start date: 2011-12-01
    End date: 2011-12-01



Possible Lamisil side effects in 60 year old female

Reported by a physician from Japan on 2012-01-31

Patient: 60 year old female

Reactions: Hepatic Function Abnormal, Hypoglycaemia

Drug(s) suspected as cause:
Glyburide
    Administration route: Oral
    Indication: Type 2 Diabetes Mellitus
    End date: 2011-12-01

Januvia
    Administration route: Oral
    Indication: Type 2 Diabetes Mellitus
    End date: 2011-12-01

Lamisil
    Administration route: Oral
    Start date: 2011-12-01
    End date: 2011-12-01



Possible Lamisil side effects in 65 year old female

Reported by a pharmacist from Japan on 2012-01-27

Patient: 65 year old female

Reactions: Hepatic Function Abnormal, Dyspnoea, Interstitial Lung Disease, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Lamisil
    Dosage: 125 mg, qd
    Administration route: Oral
    Indication: Tinea Infection
    Start date: 2011-11-09
    End date: 2011-11-22

Olopatadine HCL
    Dosage: 5 mg, qd
    Administration route: Oral
    Start date: 2011-11-09
    End date: 2011-11-22

Other drugs received by patient: Solu-Medrol; Prednisolone; Prednisolone; Prednisolone



Possible Lamisil side effects in 65 year old female

Reported by a pharmacist from Japan on 2011-12-21

Patient: 65 year old female

Reactions: Dyspnoea, Hepatic Function Abnormal, Interstitial Lung Disease, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Lamisil
    Dosage: 125 mg, qd
    Administration route: Oral
    Indication: Tinea Infection
    Start date: 2011-11-09
    End date: 2011-11-22

Olopatadine HCL
    Dosage: 5 mg, qd
    Administration route: Oral
    Start date: 2011-11-09
    End date: 2011-11-22

Other drugs received by patient: Prednisolone; Solu-Medrol; Prednisolone; Prednisolone



Possible Lamisil side effects in male

Reported by a physician from Japan on 2011-12-20

Patient: male, weighing 64.0 kg (140.8 pounds)

Reactions: Hepatic Function Abnormal, Pyrexia

Drug(s) suspected as cause:
Lamisil
    Dosage: 125 mg
    Administration route: Oral
    Indication: Tinea Pedis
    Start date: 2011-10-01
    End date: 2011-11-17

Zosyn
    Start date: 2011-11-14
    End date: 2011-11-16

Other drugs received by patient: Famotidine; Diovan; Sword; Prednisolone; Allopurinol; Tamsulosin HCL; Mestinon



Possible Lamisil side effects in female

Reported by a physician from Japan on 2011-10-19

Patient: female

Reactions: Neutrophil Percentage Increased, Blood Alkaline Phosphatase Increased, Lymphocyte Percentage Decreased, Blood Bilirubin Increased, Hepatic Function Abnormal, RED Blood Cell Count Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Concomitant Disease Aggravated, Blood Potassium Decreased, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Monocyte Percentage Decreased, Platelet Count Decreased, Blood Creatinine Increased, Blood Glucose Increased

Drug(s) suspected as cause:
Lamisil
    Dosage: unk, unk
    Indication: Tinea Pedis
    Start date: 2011-07-14

Locholest
    Dosage: 20 mg, qd
    Administration route: Oral
    Start date: 2006-01-01

Other drugs received by patient: Aricept; Uritos; Rabeprazole Sodium; Bufferin; Basen; Lasix

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