CAPOTEN Side Effects

CAPOTEN Safety Questions, CAPOTEN Answers


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CAPOTEN Safety Reports

Total CAPOTEN reports: 7.
CAPOTEN FDA safety alerts: No.
   Reported hospitalizations: 4.
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Consumer or non-health professional from BRAZIL reported CAPOTEN problem on Feb 06, 2007. Female patient, 92 years of age, was diagnosed with hypertension, blood potassium decreased and was treated with CAPOTEN. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, feeling abnormal, hypoaesthesia, muscle twitching. CAPOTEN dosage: unknown. During the same period patient was treated with HIGROTON, ALDOMET. Patient recovered.

CAPOTEN problem was reported by a Consumer or non-health professional from BRAZIL on Apr 17, 2007. Male patient, weighting 209.4 lb, was diagnosed with hypertension and was treated with CAPOTEN. After drug was administered, patient experienced the following problems/side effects: hypertension, infusion related reaction, ischaemia. CAPOTEN dosage: 50 MG QD ORAL. During the same period patient was treated with NIFEDIPINE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from BRAZIL reported CAPOTEN problem on May 18, 2007. Male patient was diagnosed with hypertension and was treated with CAPOTEN. After drug was administered, patient experienced the following problems/side effects: dizziness, dysgeusia, hypertension, malaise. CAPOTEN dosage: 150 MG QD ORAL. During the same period patient was treated with LASIX. Patient was hospitalized. Patient recovered.

CAPOTEN problem was reported by a Physician from ITALY on July 10, 2006. Male patient, 74 years of age, was diagnosed with cardiac failure and was treated with CAPOTEN. After drug was administered, patient experienced the following problems/side effects: hepatitis cholestatic, toxic skin eruption. CAPOTEN dosage: 6.25 MG TID PO. During the same period patient was treated with LASIX, NITRAKET, ACETYLSALICYLIC ACID SRT. Patient was hospitalized. Patient recovered.

Pharmacist from UNITED STATES reported CAPOTEN problem on Aug 17, 2006. Female patient, 36 years of age, was diagnosed with hypertension and was treated with CAPOTEN. After drug was administered, patient experienced the following problems/side effects: pruritus, rash, urticaria. CAPOTEN dosage: 6.25MG PO X1. Patient recovered.

CAPOTEN problem was reported by a Consumer or non-health professional from BRAZIL on Aug 11, 2006. Female patient, 56 years of age, weighting 187.4 lb, was diagnosed with hypertension and was treated with CAPOTEN. After drug was administered, patient experienced the following problems/side effects: blood pressure inadequately controlled, cerebrovascular accident, leishmaniasis. CAPOTEN dosage: unknown. During the same period patient was treated with CAPTOPRIL, HYDROCHLOROTHIAZIDE. Patient recovered.

Physician from BRAZIL reported CAPOTEN problem on Nov 30, 2006. Male patient, child 6 years of age, weighting 41.89 lb, was treated with CAPOTEN. After drug was administered, patient experienced the following problems/side effects: accidental exposure, hospitalisation, no adverse effect. CAPOTEN dosage: unknown. Patient was hospitalized. Patient recovered.

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ALABAMA
ALASKA
AMERICAN SAMOA
ARIZONA
ARKANSAS
CALIFORNIA
COLORADO
CONNECTICUT
DELAWARE
DISTRICT OF COLUMBIA
FEDERATED STATES OF MICRONESIA
FLORIDA
GEORGIA
GUAM
HAWAII
IDAHO
ILLINOIS
INDIANA
IOWA
KANSAS
KENTUCKY
LOUISIANA
MAINE
MARSHALL ISLANDS
MARYLAND
MASSACHUSETTS
MICHIGAN
MINNESOTA
MISSISSIPPI
MISSOURI
MONTANA
NEBRASKA
NEVADA
NEW HAMPSHIRE
NEW JERSEY
NEW MEXICO
NEW YORK
NORTH CAROLINA
NORTH DAKOTA
NORTHERN MARIANA ISLANDS
OHIO
OKLAHOMA
OREGON
PALAU
PENNSYLVANIA
PUERTO RICO
RHODE ISLAND
SOUTH CAROLINA
SOUTH DAKOTA
TENNESSEE
TEXAS
UTAH
VERMONT
VIRGIN ISLANDS
VIRGINIA
WASHINGTON
WEST VIRGINIA
WISCONSIN
WYOMING
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