Drug Safety Information for TEKTURNA HCT (Aliskiren hemifumarate; hydrochlorothiazide)
FDA Safety-related Labeling Changes for TEKTURNA HCT (ALISKIREN HEMIFUMARATE; HYDROCHLOROTHIAZIDE) Rx Drug: Safety Information Link
Adverse Drug Reactions for TEKTURNA HCT* (Aliskiren hemifumarate; 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 TEKTURNA HCT
(reported in FDA Medwatch/FAERS Reports)
Side Effect | # of FDA Reports | |
---|---|---|
1 | Concomitant disease progression | 52 |
2 | Renal failure acute | 37 |
3 | Dyspnoea | 36 |
4 | Dizziness | 33 |
5 | Hypotension | 32 |
6 | Renal failure | 31 |
7 | Hyperkalaemia | 29 |
8 | Blood creatinine increased | 29 |
9 | Renal impairment | 29 |
10 | Renal failure chronic | 28 |
11 | Cerebrovascular accident | 28 |
12 | Hypertension | 28 |
13 | Malaise | 28 |
14 | Blood pressure increased | 27 |
15 | Dehydration | 23 |
16 | Oedema peripheral | 22 |
17 | Cardiac failure | 21 |
18 | Nausea | 21 |
19 | Drug ineffective | 21 |
20 | Asthenia | 19 |
* This side effect also appears in "Top 10 Side Effects of TEKTURNA HCT " in the drug's Review Summary based on AskaPatient reviews.
Top 10 Reasons for Taking TEKTURNA HCT
(associated with FDA Medwatch/FAERS Reports)
Reason | # of FDA Reports | |
---|---|---|
1 | Cardiovascular disorder | 907 |
2 | Hypertension | 302 |
3 | Cardiac failure | 81 |
4 | Product used for unknown indication | 76 |
5 | Coronary artery disease | 63 |
6 | Cardiac failure chronic | 34 |
7 | Essential hypertension | 33 |
8 | Blood pressure | 20 |
9 | Blood pressure abnormal | 18 |
10 | Cardiac failure acute | 11 |
*Also a top-10 reason in AskaPatient Review Summary.
Types of Adverse Events for TEKTURNA HCT
Total Reports Filed with FDA: 2216
Number of FDA Adverse Event Reports by Patient Age for TEKTURNA HCT
Total Reports Filed with FDA: 2216*
* Reports for drugs with the same active ingredients have been aggregated in this analysis: Aliskiren hemifumarate; hydrochlorothiazide (Tekturna hct)
Charts are based on 2216 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.
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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.