BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE and SKELETAL INJURY

Overview

SKELETAL INJURY is the #14 most commonly reported adverse reaction for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE, manufactured by Gilead Sciences, Inc.. There are 2,113 FDA adverse event reports linking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE to SKELETAL INJURY. This represents approximately 3.4% of all 62,897 adverse event reports for this drug.

Patients taking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE who experience skeletal injury should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

SKELETAL INJURY is moderately reported among BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE users, representing a notable but not dominant share of adverse events.

Other Side Effects of BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE

In addition to skeletal injury, the following adverse reactions have been reported for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE:

• BONE DENSITY DECREASED — 6,535 reports
• CHRONIC KIDNEY DISEASE — 3,595 reports
• BONE LOSS — 3,431 reports
• TOOTH LOSS — 3,376 reports
• OSTEONECROSIS — 3,353 reports
• MULTIPLE FRACTURES — 3,121 reports
• RENAL FAILURE — 2,982 reports
• OSTEOPOROSIS — 2,751 reports
• PAIN — 2,531 reports
• RENAL INJURY — 2,478 reports

Other Drugs Associated with SKELETAL INJURY

The following drugs have also been linked to skeletal injury in FDA adverse event reports:

Does BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE cause SKELETAL INJURY?

SKELETAL INJURY has been reported as an adverse event in 2,113 FDA reports for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is SKELETAL INJURY with BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE?

SKELETAL INJURY accounts for approximately 3.4% of all adverse event reports for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE, making it a notable side effect.

What should I do if I experience SKELETAL INJURY while taking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE?

If you experience skeletal injury while taking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.

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