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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Misoprostol. Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (160)
Cases resulting in a serious event (72)
Cases resulting in death (5)
Cases resulting in life threatening events (11)
Cases resulting in hospitalization (60)
Cases resulting in disability (2)
Cases resulting in other serious reactions (10)
Below is a sample of reports where side effects / adverse reactions may be related to Misoprostol. For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 79 year old female receiving Misoprostol
Reported by a individual with unspecified qualification from Japan on 2007-10-31
Patient: 79 year old female
Adverse reactions / side effects: Gastrointestinal Ulcer, Haemoglobin Decreased, Large Intestinal Ulcer, Anaemia, Gastritis Erosive, Prepyloric Stenosis, Gastric Ulcer, Hepatocellular Damage
Adverse event resulted in: hospitalization
Suspect drug(s):
Diclofenac Sodium
Dosage: 50 mg/d
Indication: Back Pain
Start date: 1997-01-01
Misoprostol
Dosage: 400 ug/d
Adverse event in receiving Misoprostol
Reported by a physician from France on 2007-10-23
Patient:
Adverse reactions / side effects: Anoxia, Drug Exposure During Pregnancy, Kidney Malformation, Limb Malformation, Foetal Growth Retardation
Suspect drug(s):
Misoprostol
Adverse event in 26 year old female receiving Misoprostol
Reported by a consumer/non-health professional from United States on 2007-10-23
Patient: 26 year old female, weighing 90.7 kg (199.6 pounds)
Adverse reactions / side effects: Haemorrhage
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Misoprostol
Adverse event in 21 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 21 year old female
Adverse reactions / side effects: Haemorrhage, Abortion Incomplete
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-07-12
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-07-13
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-07-14
Adverse event in 19 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 19 year old female
Adverse reactions / side effects: Haemorrhage
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-21
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-22
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-23
Adverse event in 28 year old female receiving Misoprostol
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient: 28 year old female
Adverse reactions / side effects: Abortion Incomplete
Suspect drug(s):
Mifeprex
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-22
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-24
Adverse event in 19 year old female receiving Misoprostol
Reported by a physician from United States on 2007-10-19
Patient: 19 year old female
Adverse reactions / side effects: Haemorrhage
Suspect drug(s):
Mifeprex
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-01-31
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-02-01
End date: 2007-02-02
Adverse event in 18 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 18 year old female
Adverse reactions / side effects: Death, Vomiting, Nausea, Sepsis
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-25
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-27
Adverse event in 28 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 28 year old female
Adverse reactions / side effects: Pelvic Inflammatory Disease, Pain, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-05-31
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-01
Adverse event in 33 year old female receiving Misoprostol
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient: 33 year old female
Adverse reactions / side effects: Abortion Incomplete
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-08-25
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-08-26
Adverse event in 20 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 20 year old female
Adverse reactions / side effects: Haemorrhage, Pregnancy
Suspect drug(s):
Mifeprex
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-14
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-15
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-15
Adverse event in 37 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 37 year old female
Adverse reactions / side effects: Haemorrhage, Abortion Incomplete, Anaemia
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-04
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-05
Adverse event in 19 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 19 year old female
Adverse reactions / side effects: Uterine Haemorrhage
Suspect drug(s):
Mifeprex
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-19
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-20
Adverse event in 19 year old female receiving Misoprostol
Reported by a physician from United States on 2007-10-19
Patient: 19 year old female
Adverse reactions / side effects: Syncope, Haemorrhage, Abortion Incomplete, Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-07-30
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-07-31
Other drugs received by patient: Prophylactic Antibiotics
Adverse event in 20 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 20 year old female
Adverse reactions / side effects: Abortion Incomplete
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-08-28
Misoprostol
Dosage: 800 mcg, vaginal
Start date: 2007-08-30
Adverse event in 24 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 24 year old female
Adverse reactions / side effects: Abortion Incomplete
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2006-11-07
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-11-08
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-11-10
Adverse event in 37 year old female receiving Misoprostol
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient: 37 year old female
Adverse reactions / side effects: Haemorrhage, Abortion Incomplete, Muscle Spasms
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-07-06
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-07-07
End date: 2007-07-24
Adverse event in 30 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 30 year old female
Adverse reactions / side effects: Haemorrhage, Pain
Suspect drug(s):
Mifeprex
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-04-26
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-04-27
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-04-28
Adverse event in 18 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 18 year old female
Adverse reactions / side effects: Death, Vomiting, Nausea, Sepsis, Tachycardia, Dizziness, Rash, Muscle Spasms
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-25
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-27
Adverse event in 39 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 39 year old female
Adverse reactions / side effects: Haemorrhage, Abortion Incomplete, Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-07-19
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-07-20
Other drugs received by patient: Doxycycline; Prophylactic Antibiotics
Adverse event in 20 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 20 year old female
Adverse reactions / side effects: Haemorrhage, Abortion Incomplete, Anaemia, Chills, Dizziness
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-03-21
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-03-22
Adverse event in 26 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 26 year old female
Adverse reactions / side effects: Haemorrhage, Pain
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-08-03
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-08-04
Other drugs received by patient: Prophylactic Antibiotics
Adverse event in 25 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 25 year old female
Adverse reactions / side effects: Haemorrhage
Suspect drug(s):
Mifeprex
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-03-23
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-03-24
Adverse event in 17 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 17 year old female
Adverse reactions / side effects: Abdominal Pain, Haemorrhage, Abortion Incomplete, Muscle Spasms
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-05-14
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-05-15
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-05-30
Adverse event in 20 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 20 year old female
Adverse reactions / side effects: Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Mifepristone Tablets, 200 MG (Danco Labs)
Dosage: 200 mg, oral
Administration route: Oral
Indication: Abortion Induced
Start date: 2007-06-23
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-06-24
Other drugs received by patient: Doxycycline
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