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Protopic (Tacrolimus Topical) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (4)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Protopic (Tacrolimus Topical) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Protopic side effects in female

Reported by a physician from France on 2012-05-15

Patient: female, weighing 65.0 kg (143.0 pounds)

Reactions: Off Label Use, Acute Myeloid Leukaemia

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Protopic



Possible Protopic side effects in male

Reported by a physician from United States on 2012-04-30

Patient: male, weighing 42.0 kg (92.4 pounds)

Reactions: Obsessive-Compulsive Disorder, Tooth Extraction, Orthostatic Hypotension, Oropharyngeal Pain, Headache, Off Label Use, Autism, Burkitt's Lymphoma Stage II, Upper Respiratory Tract Infection, Melanocytic Naevus, Pharyngitis Streptococcal, Tympanic Membrane Perforation, Bronchiolitis, Cerumen Impaction, Urine Output Decreased, Otitis Media Acute, Otitis Externa, Hepatic Steatosis, Embolism Venous, Nasal Abscess, Excessive Granulation Tissue, Wrist Fracture, Tonsillitis, Fall, Constipation, Synovial Cyst, Liver Disorder, Abdominal Pain Upper, Muscle Strain, Fatigue, Pleural Effusion, Depression, Dysgraphia, Gastrooesophageal Reflux Disease, Viral Infection, Small Intestinal Bacterial Overgrowth, Radius Fracture, Abdominal Abscess, Pneumonia Bacterial, Splinter, Bronchitis, Localised Intraabdominal Fluid Collection, Infectious Peritonitis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Protopic
    Dosage: 0.1 %, bid prn
    Administration route: Topical
    Indication: Dermatitis Atopic
    Start date: 2009-01-02

Protopic
    Dosage: 0.1 %, bid prn
    Administration route: Topical
    Indication: Eczema
    Start date: 2004-01-01
    End date: 2005-01-01

Protopic
    Dosage: 0.1 %, bid
    Administration route: Topical

Other drugs received by patient possibly interacting with the suspect drug:
Elidel
    Dosage: 1 %, unknown/d
    Indication: Eczema

Other drugs received by patient: Cutivate; Bactroban; Lidex; Allegra



Possible Protopic side effects in 49 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-03

Patient: 49 year old female, weighing 81.6 kg (179.6 pounds)

Reactions: Subcutaneous Abscess, Pain, Scar

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Protopic
    Dosage: topical twice daily topical
    Administration route: Topical
    Indication: DRY Skin
    Start date: 2012-03-06
    End date: 2012-03-09

Protopic
    Dosage: topical twice daily topical
    Administration route: Topical
    Indication: Rosacea
    Start date: 2012-03-06
    End date: 2012-03-09



Possible Protopic side effects in 31 year old male

Reported by a health professional (non-physician/pharmacist) from Canada on 2011-11-02

Patient: 31 year old male, weighing 67.0 kg (147.4 pounds)

Reactions: Abdominal Discomfort, Nausea, Headache

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Protopic

Other drugs received by patient: Cold Cream; Elocon

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