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Vaseretic (Enalapril / Hydrochlorothiazide) - Fall - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Fall (2)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Vaseretic (Enalapril / Hydrochlorothiazide) where reactions include fall. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Vaseretic side effects in 82 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2012-03-08

Patient: 82 year old female

Reactions: Vomiting, Rhabdomyolysis, Hyponatraemia, Disorientation, Fall, Burns Second Degree, Diarrhoea, Asthenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Polyethylene Glycol
    Dosage: po
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2011-12-07

Depaide (Valpromide)
    Dosage: 500 mg, bid, po
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2011-12-07

Mirtazapine
    Dosage: 15 mg, qd, po
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2011-12-07

Modopar (Madopar 00349201 / )
    Dosage: 3 df, qd
    Indication: Product Used FOR Unknown Indication

Domperidone (Mfr Unknown) (Dokmperidone)
    Dosage: prn, po
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Vaseretic
    Dosage: 1 df, qd
    Indication: Product Used FOR Unknown Indication
    End date: 2011-12-07

Esomeprazole (Mfr Unknown) (Esomeprazole)
    Dosage: 20 mg, qd
    Indication: Product Used FOR Unknown Indication
    End date: 2011-12-07

Tramadol (Unknown Mfr) (Tramadol / 00599201 / )
    Dosage: prn po
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2011-12-06

Other drugs received by patient: Urbanyl



Possible Vaseretic side effects in female

Reported by a consumer/non-health professional from United States on 2011-12-06

Patient: female, weighing 118.0 kg (259.6 pounds)

Reactions: Blood Pressure Increased, Headache, Fall, Injection Site Erythema, Joint Swelling, Balance Disorder, Dehydration, Asthenia, Escherichia Infection, Renal Failure Acute

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Rebif
    Start date: 2011-08-18

Vaseretic
    Indication: Hypertension
    End date: 2011-11-01

Rebif
    Indication: Multiple Sclerosis
    Start date: 2011-05-27

Other drugs received by patient: Acetaminophen

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