Drug Safety Information for ZUTRIPRO (Chlorpheniramine maleate; hydrocodone bitartrate; pseudoephedrine hydrochloride)

FDA Safety-related Labeling Changes for ZUTRIPRO (CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE) Rx Drug: Safety Information Link

Adverse Drug Reactions for ZUTRIPRO* (Chlorpheniramine maleate; hydrocodone bitartrate; pseudoephedrine hydrochloride)

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 ZUTRIPRO
(reported in FDA Medwatch/FAERS Reports)

	Side Effect	# of FDA Reports
1	Nausea	2
2	Sinusitis	2
3	Restlessness	2
4	Vomiting	2
5	Haematocrit decreased	1
6	Therapeutic response unexpected	1
7	White blood cell count decreased	1
8	Full blood count decreased	1
9	Pain	1
10	Flushing	1
11	Haemoglobin decreased	1
12	Fall	1
13	Stomatitis	1
14	Rhinitis	1
15	Pneumonia	1
16	Pharyngitis	1
17	Heart rate increased	1
18	Pneumonitis	1
19	Nasopharyngitis	1
20	Alopecia	1

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

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

	Reason	# of FDA Reports
1	Cough	11
2	Product used for unknown indication	10
3	Bronchitis	2

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

Types of Adverse Events for ZUTRIPRO

Total Reports Filed with FDA: 41

Number of FDA Adverse Event Reports by Patient Age for ZUTRIPRO

Total Reports Filed with FDA: 41*

* Reports for drugs with the same active ingredients have been aggregated in this analysis: Chlorpheniramine maleate; hydrocodone bitartrate; pseudoephedrine hydrochloride (Zutripro)

Charts are based on 41 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.

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.