Index of reports
> Cases with Hepatitis C (5)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Zortress (Everolimus) where reactions include hepatitis c. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Zortress side effects in female
Reported by a physician from United States on 2012-05-17
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Post Transplant Lymphoproliferative Disorder, Abdominal Pain, Angina Pectoris, Hepatitis C, Liver Function Test Abnormal, Liver Transplant Rejection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Zortress
Dosage: 1 mg, bid
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-11-25
End date: 2009-12-22
Tacrolimus
Dosage: 2mg am, 1.5mg pm
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-25
End date: 2009-12-22
Prednisone TAB
Dosage: 12.5 mg, dailyk
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-24
Other drugs received by patient: Fluconazole
Possible Zortress side effects in female
Reported by a physician from United States on 2012-05-17
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Transplant Failure, Multi-Organ Failure, Renal Failure, Hepatitis C, Respiratory Failure, Liver Transplant Rejection, Hepatic Failure
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Tacrolimus
Dosage: 2mg am, 1.5mg pm
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-25
End date: 2009-12-22
Zortress
Dosage: 1 mg, bid
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-11-25
End date: 2009-12-21
Other drugs received by patient: Prednisone; Lactulose
Possible Zortress side effects in female
Reported by a physician from United States on 2012-05-17
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Post Transplant Lymphoproliferative Disorder, Abdominal Pain, Hepatitis C, Angina Pectoris, Liver Function Test Abnormal, Liver Transplant Rejection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Zortress
Dosage: 1 mg, bid
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-11-25
End date: 2009-12-22
Tacrolimus
Dosage: 2mg am, 1.5mg pm
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-25
End date: 2009-12-22
Prednisone
Dosage: 12.5 mg, dailyk
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-24
Other drugs received by patient: Fluconazole
Possible Zortress side effects in female
Reported by a physician from United States on 2012-05-16
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Abdominal Pain, Post Transplant Lymphoproliferative Disorder, Hepatitis C, Angina Pectoris, Liver Function Test Abnormal, Liver Transplant Rejection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Tacrolimus
Dosage: 2mg am, 1.5mg pm
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-25
End date: 2009-12-22
Zortress
Dosage: 1 mg, bid
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-11-25
End date: 2009-12-22
Prednisone
Dosage: 12.5 mg, dailyk
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-24
Other drugs received by patient: Fluconazole
Possible Zortress side effects in female
Reported by a physician from United States on 2012-05-16
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Abdominal Pain, Post Transplant Lymphoproliferative Disorder, Angina Pectoris, Hepatitis C, Liver Function Test Abnormal, Liver Transplant Rejection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Zortress
Dosage: 1 mg, bid
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-11-25
End date: 2009-12-22
Prednisone TAB
Dosage: 12.5 mg, dailyk
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-24
Tacrolimus
Dosage: 2mg am, 1.5mg pm
Administration route: Oral
Indication: Liver Transplant
Start date: 2009-10-25
End date: 2009-12-22
Other drugs received by patient: Fluconazole
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