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Index of reports
> Cases resulting in hospitalization (60)
> Cases with Abdominal Pain (12)
Below is the selection of adverse event reports related to Misoprostol that includes cases resulting in hospitalization where reactions include abdominal pain.
Adverse event in 27 year old female receiving Misoprostol
Reported by a physician from Germany on 2007-10-11
Patient: 27 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Tooth Fracture, Myocardial Ischaemia, Hypotension, Musculoskeletal Pain, Drug Interaction, Fall, Loss of Consciousness, Neck Pain, Heart Rate Increased, Toothache, Bradycardia, Shock
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Xyrem
Dosage: 4.5 gm (2.25 gm, 1 in 1 d), oral
Administration route: Oral
Indication: Cataplexy
Xyrem
Dosage: 4.5 gm (2.25 gm, 1 in 1 d), oral
Administration route: Oral
Indication: Narcolepsy
Misoprostol
Dosage: 2 dosage forms (2 dosage froms, 1 in 1 d), oral
Administration route: Oral
Indication: Premedication
Start date: 2007-08-28
End date: 2007-08-28
Adverse event in 39 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-20
Patient: 39 year old female
Adverse reactions / side effects: Abdominal Pain, Gastrointestinal Infection, Clostridial Infection
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: 2006-09-29
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-10-01
Adverse event in 26 year old female receiving Misoprostol
Reported by a physician from United States on 2007-07-20
Patient: 26 year old female
Adverse reactions / side effects: Abdominal Pain, Vomiting, Oedema Peripheral, 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: 2007-02-23
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-02-24
Adverse event in 33 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-15
Patient: 33 year old female
Adverse reactions / side effects: Abdominal Pain, Anaemia, Ruptured Ectopic Pregnancy
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: 2007-05-17
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-05-18
Other drugs received by patient: Propylactic Antibiotics
Adverse event in 47 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-11
Patient: 47 year old female
Adverse reactions / side effects: Abdominal Pain, Clostridial Infection
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: 2006-10-01
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-10-01
Adverse event in 39 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-11
Patient: 39 year old female
Adverse reactions / side effects: Abdominal Pain, Haemorrhage, Infection
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: 2006-09-29
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-10-01
Adverse event in 37 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-11
Patient: 37 year old female
Adverse reactions / side effects: Abdominal Pain, Ectopic Pregnancy
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: 2006-05-12
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-05-13
Adverse event in 21 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-11
Patient: 21 year old female
Adverse reactions / side effects: Abdominal Pain, Anaemia, Menorrhagia
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: 2007-01-11
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2007-01-13
Other drugs received by patient: Prophylactic Antibiotics
Adverse event in 39 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-12
Patient: 39 year old female
Adverse reactions / side effects: Abdominal Pain, Haemorrhage, Muscle Spasms, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Mifeprex
Misoprostol
Adverse event in 47 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-17
Patient: 47 year old female
Adverse reactions / side effects: Abdominal Pain, Clostridial Infection
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: 2006-09-29
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-10-01
Adverse event in 39 year old female receiving Misoprostol
Reported by a individual with unspecified qualification from United States on 2007-01-24
Patient: 39 year old female
Adverse reactions / side effects: Abdominal Pain, Haemorrhage, Muscle Spasms, Infection
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: 2006-09-29
Misoprostol
Dosage: 800 mcg, buccal
Start date: 2006-10-01
Adverse event in 39 year old female receiving Misoprostol
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-01-11
Patient: 39 year old female
Adverse reactions / side effects: Abdominal Pain, Laparotomy, Uterine Rupture
Adverse event resulted in: hospitalization
Suspect drug(s):
Syntocinon
Mifepristone
Dosage: 200 mg, unk
Misoprostol
Dosage: 800 ug/day
Misoprostol
Dosage: 400 ug/day
Administration route: Oral
Gemeprost
Dosage: 1 mg/day
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