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Kenalog (Triamcinolone Topical) - Contusion - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Contusion (4)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Kenalog (Triamcinolone Topical) where reactions include contusion. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Kenalog side effects in 52 year old female

Reported by a consumer/non-health professional from United States on 2012-08-01

Patient: 52 year old female, weighing 59.0 kg (129.8 pounds)

Reactions: Contusion, Vasodilatation, Wound Haemorrhage, Skin Atrophy

Drug(s) suspected as cause:
Kenalog



Possible Kenalog side effects in 70 year old female

Reported by a consumer/non-health professional from United States on 2012-05-03

Patient: 70 year old female, weighing 68.0 kg (149.7 pounds)

Reactions: Contusion, Goitre, Neck Pain, Skin Discolouration, Thyroid Disorder, Exercise Tolerance Decreased, Spinal Column Stenosis

Drug(s) suspected as cause:
Kenalog
    Start date: 2008-07-24
    End date: 2009-04-01

Plavix
    Start date: 2009-06-01
    End date: 2010-07-01

Plavix
    Indication: Stent Placement
    Start date: 2009-06-01
    End date: 2010-07-01



Possible Kenalog side effects in 65 year old male

Reported by a consumer/non-health professional from United States on 2012-02-22

Patient: 65 year old male, weighing 91.0 kg (200.2 pounds)

Reactions: Contusion

Drug(s) suspected as cause:
Kenalog

Other drugs received by patient: Nexium; Biotin; Exforge HCT; Bystolic; Dexlansoprazole; Vitamin TAB



Possible Kenalog side effects in 64 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2011-12-23

Patient: 64 year old female

Reactions: Injection Site Discolouration, Wrong Technique in Drug Usage Process, Pruritus, Contusion, Injection Site Haemorrhage, Injection Site Haematoma, Wound, Skin Discolouration, Injection Site Extravasation, Injection Site Reaction, Drug Administration Error, Product Quality Issue, Injection Site Scar, Hypoaesthesia, Paraesthesia, Meralgia Paraesthetica, Injection Site Anaesthesia

Drug(s) suspected as cause:
Kenalog
    Dosage: 20 mg/ 0.5cc x 8
    Indication: Urticaria
    Start date: 2009-01-01
    End date: 2011-03-11

Dexamethasone Sodium Phosphate
    Dosage: 120 mg/ 0.5cc x 8
    Indication: Urticaria
    Start date: 2009-01-01
    End date: 2011-03-11

Other drugs received by patient: Tenormin; Premarin

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