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Index of reports
> Cases resulting in hospitalization (7)
Below is the selection of adverse event reports related to Zestoretic (Lisinopril / Hydrochlorothiazide) that includes cases resulting in hospitalization.
Adverse event in male receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-17
Patient: male, weighing 89.0 kg (195.8 pounds)
Adverse reactions / side effects: Pancreatitis Acute, Respiratory Failure, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zestoretic (Lisinopril / Hydrochlorothiazide)
Other drugs received by patient: Tahor; Seretide
Adverse event in 65 year old male receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-07-03
Patient: 65 year old male
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: hospitalization
Suspect drug(s):
Fonzylane
Administration route: Oral
Indication: Arteritis
Start date: 2003-06-15
Novatrex
Dosage: 20 mg weekly
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 1997-01-15
End date: 2007-03-25
Plavix
Administration route: Oral
Indication: Arteritis
Start date: 2003-03-15
Zestoretic
Administration route: Oral
Indication: Hypertension
Start date: 2003-01-15
End date: 2007-04-16
Adverse event in 65 year old male receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-29
Patient: 65 year old male
Adverse reactions / side effects: Weight Decreased, Dyspnoea Exertional, Interstitial Lung Disease, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Fonzylane
Dosage: unk
Administration route: Oral
Indication: Arteritis Obliterans
Start date: 2003-06-15
Novatrex
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 1997-01-15
End date: 2007-03-25
Plavix
Dosage: unk
Administration route: Oral
Indication: Arteritis Obliterans
Start date: 2003-03-15
Zestoretic
Dosage: unk
Administration route: Oral
Indication: Hypertension
Start date: 2003-01-15
End date: 2007-04-16
Adverse event in 77 year old male receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-11
Patient: 77 year old male, weighing 76.0 kg (167.2 pounds)
Adverse reactions / side effects: Coagulation Factor Viii Level Decreased, Coagulation Time Prolonged, Haematoma
Adverse event resulted in: hospitalization
Suspect drug(s):
Tanakan
Administration route: Oral
Vioxx
Administration route: Oral
Start date: 2004-02-15
End date: 2004-06-10
Zestoretic
Administration route: Oral
Zocor
Administration route: Oral
Adverse event in 52 year old female receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a consumer/non-health professional from United States on 2007-02-01
Patient: 52 year old female
Adverse reactions / side effects: Pruritus, Larynx Irritation, Urticaria, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Coaprovel
Administration route: Oral
Start date: 2006-11-22
End date: 2006-11-26
Lisinopril and Hydrochlorothiazide
Start date: 2006-10-04
End date: 2006-11-18
Zestoretic
Administration route: Oral
Start date: 2002-06-15
End date: 2006-11-22
Adverse event in female receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-25
Patient: female
Adverse reactions / side effects: Respiratory Disorder, Urticaria, Erythema, Malaise, Throat Irritation, Feeling Hot, Oedema, Prurigo, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Coaprovel
Administration route: Oral
Start date: 2006-11-22
End date: 2006-11-26
Lisinopril + Hydrochlorothiazide Arrow
Administration route: Oral
Start date: 2006-10-04
End date: 2006-11-18
Zestoretic
Dosage: 20 + 12.5 mg daily
Administration route: Oral
Start date: 2002-06-15
End date: 2006-10-04
Zestoretic
Dosage: 20 + 12.5 mg daily
Administration route: Oral
Start date: 2006-11-20
End date: 2006-11-22
Adverse event in female receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-18
Patient: female
Adverse reactions / side effects: Throat Irritation, Urticaria, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Coaprovel
Administration route: Oral
Start date: 2006-11-22
End date: 2006-11-26
Lisinopril + Hydrochlorothiazide Arrow
Administration route: Oral
Start date: 2006-10-04
End date: 2006-11-18
Zestoretic
Dosage: 20 + 12.5 mg daily
Administration route: Oral
Start date: 2002-06-15
End date: 2006-10-04
Zestoretic
Dosage: 20 + 12.5 mg daily
Administration route: Oral
Start date: 2006-11-20
End date: 2006-11-22
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