Drug Safety Information for CORZIDE (Bendroflumethiazide; nadolol)

Safety-related Labeling Changes for CORZIDE (BENDROFLUMETHIAZIDE; NADOLOL) Rx Drug: FDA Link

Adverse Drug Reactions for CORZIDE* (Bendroflumethiazide; nadolol)

These charts and graphs are based on reports received through the FDA Adverse Event Reporting System (FAERS) program (see below).

Top 20 Adverse Effects Associated with CORZIDE
(reported in FDA Medwatch/FAERS Reports)

  Side Effect # of FDA Reports
1Dyspnoea6
2Rash5
3Renal failure acute4
4Back pain4
5Fatigue4
6Arthralgia4
7Depression3
8Anxiety3
9Muscle spasms3
10Dizziness*3
11Osteoarthritis3
12Crepitations3
13Alopecia3
14Arrhythmia3
15Atrial fibrillation3
16Lower respiratory tract infection3
17Breast cancer female3
18Hyperglycaemia3
19Pain3
20Hypertension3

* This side effect also appears in "Top 10 Side Effects of CORZIDE " in the drug's Review Summary based on AskaPatient reviews.

Top 10 Reasons for Taking CORZIDE
(associated with FDA Medwatch/FAERS Reports)

Reason # of FDA Reports
1Hypertension*127
2Product used for unknown indication8
3Blood pressure8

*Also a top-10 reason in AskaPatient Review Summary.


Types of Adverse Events for CORZIDE

Total Reports Filed with FDA: 354


Number of FDA Adverse Event Reports by Patient Age for CORZIDE

Total Reports Filed with FDA: 354*


* Reports for drugs with the same active ingredients have been aggregated in this analysis: Bendroflumethiazide; nadolol (Corzide)

Charts are based on 354 reports filed with the FDA between 2004 and June 2015.

Adverse Event Reports are submitted to the FDA by pharmaceutical companies (mandatory reporting is required by manufacturers, distributors, or importers), health care providers such as doctors (voluntary reporting), and by patients themselves (voluntary reporting). More Information on FDA MedWatch (FDA Safety Information and Adverse Event Reporting Program)Voluntary reporting takes place under the FDA's MedWatch program, where health care professionals and consumers submit reports to FDA when they find a problem with a drug, medical device, biologic, or other FDA-regulated product. An adverse event is any undesirable experience or extreme side effect associated with the use of a medical product. Adverse events include: death, life threatening event, hospitalization, disability or permanent damage, congenital anomaly or birth defect, medical product use requiring a surgical or other intervention, or other serious medical situation believed to be caused by the drug.

Click to go back to search results and CORZIDE Reviews and Review Summary .

Historical Analytics of FDA Adverse Event Reports Provided by Druginformer.com. FDA Drug Safety Information, including safety-related labeling updates, required post-approval safety studies, risk evaluation management strategies (REMS), alerts, and recalls are compiled by AskaPatient.com from the U.S. Food and Drug Administration.