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Protopic (Tacrolimus Topical) - Myocardial Infarction - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Myocardial Infarction (4)

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

Possible Protopic side effects in 47 year old female

Reported by a pharmacist from Japan on 2012-01-06

Patient: 47 year old female

Reactions: Blood Potassium Decreased, Myocardial Infarction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Infree
    Indication: Product Used FOR Unknown Indication

Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Indication: Pain
    Start date: 2011-11-16

Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Start date: 2011-10-12
    End date: 2011-11-15

Prednisolone
    Indication: Product Used FOR Unknown Indication

Infree
    Dosage: as needed

Protopic
    Indication: Product Used FOR Unknown Indication
    End date: 2011-10-21

Diclofenac Sodium
    Indication: Product Used FOR Unknown Indication

Other drugs received by patient: Unknown Multiple Medication



Possible Protopic side effects in 47 year old female

Reported by a pharmacist from Japan on 2011-12-21

Patient: 47 year old female

Reactions: Blood Potassium Decreased, Myocardial Infarction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Protopic
    Indication: Product Used FOR Unknown Indication
    End date: 2011-10-21

Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Indication: Pain
    Start date: 2011-11-16

Prednisolone
    Indication: Product Used FOR Unknown Indication

Infree
    Indication: Product Used FOR Unknown Indication

Diclofenac Sodium
    Indication: Product Used FOR Unknown Indication

Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Start date: 2011-10-12
    End date: 2011-11-15

Infree
    Dosage: as needed

Other drugs received by patient: Unknown Multiple Medication



Possible Protopic side effects in 47 year old female

Reported by a pharmacist from Japan on 2011-12-15

Patient: 47 year old female

Reactions: Blood Potassium Decreased, Myocardial Infarction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Start date: 2011-10-12
    End date: 2011-11-15

Prednisolone
    Indication: Product Used FOR Unknown Indication

Infree
    Dosage: as needed

Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Indication: Pain
    Start date: 2011-11-16

Protopic
    Indication: Product Used FOR Unknown Indication
    End date: 2011-10-21

Infree
    Indication: Product Used FOR Unknown Indication

Diclofenac Sodium
    Indication: Product Used FOR Unknown Indication

Other drugs received by patient: Unknown Multiple Medication



Possible Protopic side effects in 47 year old female

Reported by a pharmacist from Japan on 2011-12-12

Patient: 47 year old female

Reactions: Blood Potassium Decreased, Myocardial Infarction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Infree
    Indication: Product Used FOR Unknown Indication

Infree
    Dosage: as needed

Diclofenac Sodium
    Indication: Product Used FOR Unknown Indication

Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Start date: 2011-10-12
    End date: 2011-11-15

Prednisolone
    Indication: Product Used FOR Unknown Indication

Tramadol Hydrochloride / Acetaminophen
    Dosage: 1 per day
    Administration route: Oral
    Indication: Pain
    Start date: 2011-11-16

Protopic
    Indication: Product Used FOR Unknown Indication
    End date: 2011-10-21

Other drugs received by patient: Unknown Multiple Medication

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