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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Zestoretic (Lisinopril / Hydrochlorothiazide). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view all available reports.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (9)
Cases resulting in a serious event (8)
Cases resulting in life threatening events (1)
Cases resulting in hospitalization (7)
Cases resulting in other serious reactions (1)
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 female receiving Zestoretic (Lisinopril / Hydrochlorothiazide)
Reported by a physician from United States on 2007-04-30
Patient: female, weighing 102.5 kg (225.5 pounds)
Adverse reactions / side effects: Headache
Suspect drug(s):
Lisinopril
Dosage: 20/25 1 po q day 1 po q daily po
Indication: Hypertension
Start date: 1996-06-01
End date: 1997-07-01
Zestoretic
Dosage: 20/25 1 po q day 1 po q daily po
Administration route: Oral
Indication: Hypertension
Start date: 1996-06-01
End date: 1997-07-01
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 physician from Belgium on 2007-01-24
Patient: female
Adverse reactions / side effects: Urinary Retention, Feeling Abnormal
Suspect drug(s):
Zestoretic (Lisinopril / Hydrochlorothiazide)
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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