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Progesterone (Progesterone) - Jaundice - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Jaundice (6)

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

Possible Progesterone side effects in female

Reported by a health professional (non-physician/pharmacist) from France on 2012-05-09

Patient: female

Reactions: Jaundice, Asterixis, Encephalopathy, Hepatic Failure, Hepatitis Toxic, Liver Disorder

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Progesterone
    Administration route: Oral
    Indication: Hormone Replacement Therapy

Escitalopram
    Indication: Major Depression

Disulfiram
    Indication: Alcoholism
    Start date: 2011-05-01
    End date: 2011-06-01

Other drugs received by patient: Oxazepam; Levothyroxine Sodium; Estradiol; Milnacipran



Possible Progesterone side effects in female

Reported by a health professional (non-physician/pharmacist) from Denmark on 2012-05-09

Patient: female

Reactions: Jaundice, Asterixis, Hepatic Failure, Encephalopathy, Hepatitis Toxic, Liver Disorder

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Progesterone
    Administration route: Oral
    Indication: Hormone Replacement Therapy

Escitalopram
    Indication: Major Depression

Disulfiram
    Indication: Alcoholism
    Start date: 2011-05-01
    End date: 2011-06-01

Other drugs received by patient: Levothyroxine Sodium; Milnacipran; Oxazepam; Estradiol



Possible Progesterone side effects in female

Reported by a health professional (non-physician/pharmacist) from France on 2012-04-30

Patient: female

Reactions: Jaundice, Asterixis, Encephalopathy, Hepatic Failure, Hepatitis Toxic, Liver Disorder

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Progesterone
    Administration route: Oral
    Indication: Hormone Replacement Therapy

Esperal
    Indication: Alcoholism
    Start date: 2011-05-01
    End date: 2011-06-01

Escitalopram
    Indication: Major Depression

Other drugs received by patient: Oxazepam; Estreva; Ixel; Levothyroxine Sodium



Possible Progesterone side effects in female

Reported by a physician from Singapore on 2011-11-30

Patient: female

Reactions: Abdominal Discomfort, Jaundice, Overdose, Ocular Icterus, Hepatic Enzyme Increased

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Progesterone
    Dosage: once
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-10-08
    End date: 2011-10-08

Progesterone
    Dosage: 200 mg (100 mg, 2 in 1 d)
    Administration route: Oral
    Indication: Menorrhagia
    Start date: 2011-10-09
    End date: 2011-10-10

Tranexamic Acid
    Indication: Menorrhagia

Other drugs received by patient: Tranexamic Acid



Possible Progesterone side effects in 53 year old female

Reported by a pharmacist from Canada on 2011-11-21

Patient: 53 year old female

Reactions: Confusional State, Jaundice, Spider Naevus, Hepatic Necrosis, Autoimmune Hepatitis, Toxicity To Various Agents, Ascites, Fatigue, Asterixis, Hepatic Encephalopathy, Hepatic Cirrhosis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Budesonide / Formoterol Fumarate Dihydrate
    Dosage: 200/6 mcg;bid

Acidophilus with Bifidus (NO Pref. Name)
    Dosage: tid;po
    Start date: 2008-11-01
    End date: 2009-04-01

Conjugated Linoleic Acid (NO Pref. Name)
    Dosage: tid;po
    Start date: 2008-11-01
    End date: 2009-04-01

GHR Homan Growth Hormone (NO Pref. Name)
    Start date: 2008-10-01
    End date: 2009-01-01

Nutriminc (NO Pref. Name)
    Dosage: capsules;bid;po
    Administration route: Oral
    Start date: 2008-11-01
    End date: 2009-04-01

Venlafaxine HCL
    Dosage: 150 mg

Progesterone
    Dosage: 100 mg
    End date: 2009-04-01

Methylsolfonylmethane (NO Pref. Name)
    Dosage: qd-tid;
    Start date: 2008-11-01
    End date: 2009-04-01

Softcap Fish OIL (NO Pref. Name)
    Dosage: bid; po
    Administration route: Oral
    Start date: 2008-11-01
    End date: 2009-04-01

Varenicline
    Dosage: 0.5 mg;qd
    Start date: 2008-12-01
    End date: 2009-04-01

Estraderm
    Dosage: 50 mcg/d;q2w
    End date: 2009-04-01

Lorazepam
    Dosage: 1 mg;qd
    End date: 2009-04-01

Other drugs received by patient: Vitamin D (NO Pref. Name)



Possible Progesterone side effects in female

Reported by a physician from Singapore on 2011-11-17

Patient: female

Reactions: Abdominal Discomfort, Jaundice, Ocular Icterus, Pyrexia, Hepatic Enzyme Increased

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Progesterone
    Dosage: once
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-10-08
    End date: 2011-10-08

Tranexamic Acid
    Indication: Menorrhagia

Progesterone
    Dosage: 200 mg (100 mg, 2 in 1 d)
    Administration route: Oral
    Indication: Menorrhagia
    Start date: 2011-10-09
    End date: 2011-10-10

Other drugs received by patient: Tranexamic Acid

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