Drug Safety Information for HYDRODIURIL (Hydrochlorothiazide)

Safety-related Labeling Changes for ALDACTAZIDE (HYDROCHLOROTHIAZIDE; SPIRONOLACTONE) Rx Drug: FDA Link

Safety-related Labeling Changes for DYAZIDE (HYDROCHLOROTHIAZIDE; TRIAMTERENE) Rx Drug: FDA Link

Safety-related Labeling Changes for LOPRESSOR HCT (HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE) Rx Drug: FDA Link

Safety-related Labeling Changes for MAXZIDE (HYDROCHLOROTHIAZIDE; TRIAMTERENE) Rx Drug: FDA Link

Safety-related Labeling Changes for MAXZIDE-25 (HYDROCHLOROTHIAZIDE; TRIAMTERENE) Rx Drug: FDA Link

Safety-related Labeling Changes for ZESTORETIC (HYDROCHLOROTHIAZIDE; LISINOPRIL) Rx Drug: FDA Link

Safety-related Labeling Changes for ACCURETIC (HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE) Rx Drug: FDA Link

Safety-related Labeling Changes for HYZAAR (HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM) Rx Drug: FDA Link

Safety-related Labeling Changes for MICROZIDE (HYDROCHLOROTHIAZIDE) Rx Drug: FDA Link

Safety-related Labeling Changes for AVALIDE (HYDROCHLOROTHIAZIDE; IRBESARTAN) Rx Drug: FDA Link

Safety-related Labeling Changes for DIOVAN HCT (HYDROCHLOROTHIAZIDE; VALSARTAN) Rx Drug: FDA Link

Safety-related Labeling Changes for MICARDIS HCT (HYDROCHLOROTHIAZIDE; TELMISARTAN) Rx Drug: FDA Link

Safety-related Labeling Changes for BENICAR HCT (HYDROCHLOROTHIAZIDE: OLMESARTAN MEDOXOMIL) Rx Drug: FDA Link

Safety-related Labeling Changes for DUTOPROL (HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE) Rx Drug: FDA Link

Adverse Drug Reactions for HYDRODIURIL* (Hydrochlorothiazide)

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 HYDRODIURIL
(reported in FDA Medwatch/FAERS Reports)

  Side Effect # of FDA Reports
1Nausea3540
2Dizziness*2886
3Dyspnoea2816
4Drug ineffective2733
5Fatigue*2726
6Pain*2418
7Diarrhoea2377
8Headache*2256
9Asthenia2224
10Hypertension2057
11Vomiting2012
12Fall1767
13Arthralgia*1667
14Pain in extremity1642
15Oedema peripheral1605
16Anxiety1532
17Chest pain1496
18Hypotension1443
19Depression1416
20Back pain1396

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

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

Reason # of FDA Reports
1Hypertension*39481
2Product used for unknown indication18435
3Blood pressure*3899
4Fluid retention*2088
5Diuretic therapy2026
6Blood pressure abnormal1302
7Oedema*959
8Blood pressure increased760
9Oedema peripheral690
10Essential hypertension578

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


Types of Adverse Events for HYDRODIURIL

Total Reports Filed with FDA: 257277


Number of FDA Adverse Event Reports by Patient Age for HYDRODIURIL

Total Reports Filed with FDA: 257277*


* Reports for drugs with the same active ingredients have been aggregated in this analysis: Hydrochlorothiazide (Carozide, Hydro-d, Hydrocot, Microzide, Hypothiazide, Zide, Hydrochlorothiazide, Esidrix, Oretic, Hydrodiuril)

Charts are based on 257277 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 HYDRODIURIL 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.