Drug Information
Ingredients:
  • Hydrocodone Bitartrate; Ibuprofen
Drug Brands and Names:
  • Hydrocodone Bitartrate And Ibuprofen
  • Hydrocodone Bitartrate; Ibuprofen
  • Ibudone
  • Reprexain
  • Vicoprofen
Manufacturers:
  • Abbvie Inc.
  • Aidarex Pharmaceuticals Llc
  • Gemini Laboratories, Llc
  • Poly Pharmaceuticals
Approved Uses (Extracted from drug label):
  • No data available
Common Uses (Extracted from FDA adverse event reports):
Side Effect Information
Preferred Term: Abdominal Pain Upper
Additional Terms:
  • Stomach pain
  • Stomach cramps
  • Stomach ache
  • Epigastric pain
  • Severe pain in my stomach
  • Cramp stomach
  • painful cramps in my stomach
  • Pain stomach
  • Pancreatic pain
  • Abdominal pain, upper
  • Upper abdominal pain
  • Gastric pain
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Hydrocodone Bitartrate; Ibuprofen Related Abdominal Pain Upper

  • Official FDA
    Reports
  • Social Media
    Reports

Hydrocodone Bitartrate; Ibuprofen Related Abdominal Pain Upper Age and Gender Distribution (From AERS Data)


Trends in Hydrocodone Bitartrate; Ibuprofen Related Abdominal Pain Upper Adverse Event Reports

AERS Reports (FDA)
Social Media Reports

Hydrocodone Bitartrate; Ibuprofen Related Abdominal Pain Upper Reports (From AERS Data)

* "-" Indicates fields that were not specified in report recieved by the FDA.

Hydrocodone Bitartrate; Ibuprofen Related Abdominal Pain Upper Reports (From Social Media - User Reviews and Forum Discussions)


Ade SMM Report
* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About AERS: The Adverse Event Reporting System (AERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into AERS. The AERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, AERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.
The total number of adverse event reports in the FDA-owned Adverse Event Reporting System (AERS).
The total number of adverse event reports extracted from online social media sources (forum discussions, user reviews, etc).