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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