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Lidocaine (Lidocaine) - Incorrect Route of Drug Administration - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Incorrect Route of Drug Administration ()

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Lidocaine where reactions include incorrect route of drug administration. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Lidocaine side effects in 24 year old male

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-01-27

Patient: 24 year old male

Reactions: Incorrect Route of Drug Administration, Exophthalmos, Mydriasis, Vitreous Floaters, Intraocular Pressure Increased, Blindness Unilateral, Eye Pain

Drug(s) suspected as cause:
Lidocaine



Possible Lidocaine side effects in male

Reported by a consumer/non-health professional from United States on 2012-01-02

Patient: male, weighing 73.9 kg (162.6 pounds)

Reactions: Incorrect Route of Drug Administration, Wrong Technique in Drug Usage Process, Pain in Extremity, Nausea, Septic Arthritis Staphylococcal, Motor Dysfunction, Pain, Myalgia, Off Label Use, Fatigue

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Optiray 160
    Dosage: 5-10 ml
    Indication: X-RAY
    Start date: 2009-04-29
    End date: 2009-04-29

Lidocaine
    Dosage: 5 ml, single
    Indication: X-RAY
    Start date: 2009-04-29
    End date: 2009-04-29

Sodium Chloride
    Dosage: 10 ml, single
    Indication: Arthrogram
    Start date: 2009-04-29
    End date: 2009-04-29

Magnevist
    Dosage: 1 ml, single
    Indication: Arthrogram
    Start date: 2009-04-29
    End date: 2009-04-29



Possible Lidocaine side effects in female

Reported by a health professional (non-physician/pharmacist) from Germany on 2011-12-20

Patient: female, weighing 108.0 kg (237.6 pounds)

Reactions: Ligament Injury, Procedural Pain, Incorrect Route of Drug Administration, Wrong Technique in Drug Usage Process, Septic Arthritis Staphylococcal, Fall, Off Label Use, Joint Swelling, Arthralgia, Gait Disturbance, Lymphoedema, Normochromic Normocytic Anaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sodium Chloride
    Dosage: 10 ml, single
    Indication: Arthrogram
    Start date: 2009-04-29
    End date: 2009-04-29

Magnevist
    Dosage: 1 ml, single
    Indication: Arthrogram
    Start date: 2009-04-29
    End date: 2009-04-29

Magnevist
    Indication: Joint Injury

Lidocaine
    Dosage: 5 ml, single
    Indication: X-RAY
    Start date: 2009-04-29
    End date: 2009-04-29

Optiray 160
    Dosage: 5-10 ml
    Indication: X-RAY
    Start date: 2009-04-29
    End date: 2009-04-29

Other drugs received by patient: Soma; Naprosyn; Vicodin; Ambien; Buspirone HCL; Risperdal



Possible Lidocaine side effects in 38 year old female

Reported by a physician from India on 2011-11-08

Patient: 38 year old female, weighing 50.0 kg (110.0 pounds)

Reactions: Neurotoxicity, Incorrect Route of Drug Administration, Cardio-Respiratory Arrest, Convulsion

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Lidocaine
    Indication: Epidural Anaesthesia

Epinephrine
    Indication: Epidural Anaesthesia

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