Drug Safety Information for TIROSINT (Levothyroxine sodium)
FDA Safety-related Labeling Changes for THYRO-TABS (LEVOTHYROXINE SODIUM) Rx Drug: Safety Information Link
FDA Safety-related Labeling Changes for UNITHROID (LEVOTHYROXINE SODIUM) Rx Drug: Safety Information Link
FDA Safety-related Labeling Changes for LEVO-T (LEVOTHYROXINE SODIUM) Rx Drug: Safety Information Link
FDA Safety-related Labeling Changes for SYNTHROID (LEVOTHYROXINE SODIUM) Rx Drug: Safety Information Link
FDA Safety-related Labeling Changes for TIROSINT (LEVOTHYROXINE SODIUM) Rx Drug: Safety Information Link
FDA Safety-related Labeling Changes for TIROSINT-SOL (LEVOTHYROXINE SODIUM) Rx Drug: Safety Information Link
Adverse Drug Reactions for TIROSINT* (Levothyroxine sodium)
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 TIROSINT
(reported in FDA Medwatch/FAERS Reports)
Side Effect | # of FDA Reports | |
---|---|---|
1 | Nausea | 11637 |
2 | Fatigue* | 10607 |
3 | Drug ineffective | 10165 |
4 | Dyspnoea | 8980 |
5 | Headache* | 8666 |
6 | Dizziness | 8460 |
7 | Diarrhoea | 8417 |
8 | Pain | 7488 |
9 | Asthenia | 7047 |
10 | Vomiting | 6435 |
11 | Fall | 6073 |
12 | Arthralgia* | 5756 |
13 | Malaise | 5589 |
14 | Pain in extremity | 5296 |
15 | Weight decreased | 4947 |
16 | Insomnia* | 4868 |
17 | Anxiety* | 4690 |
18 | Pruritus | 4680 |
19 | Rash | 4678 |
20 | Depression* | 4345 |
* This side effect also appears in "Top 10 Side Effects of TIROSINT " in the drug's Review Summary based on AskaPatient reviews.
Top 10 Reasons for Taking TIROSINT
(associated with FDA Medwatch/FAERS Reports)
Reason | # of FDA Reports | |
---|---|---|
1 | Hypothyroidism* | 143943 |
2 | Product used for unknown indication | 82010 |
3 | Thyroid disorder | 52013 |
4 | Thyroidectomy* | 6195 |
5 | Autoimmune thyroiditis* | 5473 |
6 | Hyperthyroidism | 3932 |
7 | Basedow's disease | 1570 |
8 | Thyroid hormone replacement therapy | 1379 |
9 | Hormone replacement therapy | 1359 |
10 | Blood thyroid stimulating hormone decreased | 1083 |
*Also a top-10 reason in AskaPatient Review Summary.
Types of Adverse Events for TIROSINT
Total Reports Filed with FDA: 804746
Number of FDA Adverse Event Reports by Patient Age for TIROSINT
Total Reports Filed with FDA: 804746*
* Reports for drugs with the same active ingredients have been aggregated in this analysis: Levothyroxine sodium (L-thyrox, Levotabs, L-thyroxine roche, Levothyroxine, Novothyrox, Dexnon, Euthyrox, T4, Levotiroxina sodica, Eutirox, Thyroxine, Sodium levothyroxine, Thyrax, Oroxine, Berlthyrox, Tirosint, Thyroxine sodium, Thyroxin, L-thyroxin henning, Novothyral, Levoxine, Levothyrox, Eltroxin, Tiroxina, Eltroxine, L thyroxine, L-thyroxine, Thyrox, Levothyroid, Eferox, Levoxyl, Levothyroxine sodium, Unithroid, Synthroid, Levolet, Tiroxina sodica, Levo-t, Levothroid)
Charts are based on 804746 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 TIROSINT 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.