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Aldomet Side Effects Report #5478420-6
Physician from JAPAN reported ALDOMET problem on Sept 28, 2007. Male patient, weighting 4.41 lb, was treated with ALDOMET. After drug was administered, patient experienced the following problems/side effects: foetal disorder, respiratory disorder, . ALDOMET dosage: unknown. During the same period patient was treated with AMLODIPINE BESYLATE. Patient recovered.

Aldomet Side Effects Report #5493943-1
ALDOMET problem was reported by a Physician from JAPAN on Sept 19, 2007. Male patient, weighting 4.41 lb, was treated with ALDOMET. After drug was administered, patient experienced the following problems/side effects: foetal disorder, respiratory disorder, . ALDOMET dosage: unknown. During the same period patient was treated with AMLODIPINE BESYLATE. Patient recovered.

Aldomet Side Effects Report #5470928-2
Physician from JAPAN reported ALDOMET problem on Sept 19, 2007. Male patient, weighting 4.41 lb, was treated with ALDOMET. After drug was administered, patient experienced the following problems/side effects: foetal disorder, respiratory disorder, . ALDOMET dosage: unknown. During the same period patient was treated with AMLODIPINE BESYLATE. Patient recovered.

Sustiva Side Effects Report #5656555-2
SUSTIVA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 05, 2008. Female patient, 33 years of age, was diagnosed with hiv infection and was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: abortion induced, foetal disorder, pregnancy, . SUSTIVA dosage: unknown. During the same period patient was treated with NEVIRAPINE, KIVEXA, COMBIVIR, KALETRA. Patient recovered.


Hyzaar Side Effects Report #5662273-7
Health Professional from SWITZERLAND reported HYZAAR problem on Mar 07, 2008. Female patient, 41 years of age, was diagnosed with essential hypertension and was treated with HYZAAR. After drug was administered, patient experienced the following problems/side effects: foetal disorder, . HYZAAR dosage: unknown. During the same period patient was treated with LISINOPRIL, ATENOLOL, SPIRONOLACTONE, ASPIRIN. Patient recovered.

Aldactone Side Effects Report #5671551-7
ALDACTONE problem was reported by a Physician from SWITZERLAND on Mar 06, 2008. Female patient was diagnosed with essential hypertension and was treated with ALDACTONE. After drug was administered, patient experienced the following problems/side effects: foetal disorder, . ALDACTONE dosage: DAILY DOSE:25MG. During the same period patient was treated with ATENOLOL, LISINOPRIL, COSAAR PLUS, ASPIRIN. Patient recovered.

Aspirin Side Effects Report #5679028-X
Physician from SWITZERLAND reported ASPIRIN problem on Mar 10, 2008. Female patient, 41 years of age, was diagnosed with hypertension, essential hypertension and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: foetal disorder, pregnancy, renal failure, . ASPIRIN dosage: unknown. During the same period patient was treated with LISITRIL, COSAAR PLUS, ATENOLOL, ALDACTONE. Patient recovered.

Aldactone Side Effects Report #5683356-1
ALDACTONE problem was reported by a Physician from SWITZERLAND on Mar 17, 2008. Female patient was diagnosed with essential hypertension and was treated with ALDACTONE. After drug was administered, patient experienced the following problems/side effects: foetal disorder, . ALDACTONE dosage: DAILY DOSE:25MG. During the same period patient was treated with ATENOLOL, LISINOPRIL, COSAAR PLUS, ASPIRIN. Patient recovered.

Effexor Side Effects Report #5636214-2
Health Professional from SWITZERLAND reported EFFEXOR problem on Feb 13, 2008. Female patient, 27 years of age, was diagnosed with depression, hypothyroidism, schizophrenia, essential hypertension, hyperlipidaemia and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: foetal disorder, . EFFEXOR dosage: unknown. During the same period patient was treated with ELTROXIN, XANAX, QUETIAPINE FUMARATE, BELOC ZOK, SORTIS. Patient was hospitalized. Patient recovered.


Sustiva Side Effects Report #5602649-7
SUSTIVA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 24, 2008. Female patient, 33 years of age, was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: abortion induced, foetal disorder, pregnancy, . SUSTIVA dosage: unknown. During the same period patient was treated with NEVIRAPINE. Patient recovered.

Propess Side Effects Report #5575689-4
Consumer or non-health professional from UNITED KINGDOM reported PROPESS problem on Dec 14, 2007. Female patient was diagnosed with labour induction and was treated with PROPESS. After drug was administered, patient experienced the following problems/side effects: foetal disorder, foetal distress syndrome, haematoma, placental disorder, . PROPESS dosage: 10 MG ONCE VG. Patient died.

Valacyclovir Side Effects Report #5468181-9
VALACYCLOVIR problem was reported by a Consumer or non-health professional from FRANCE on Sept 10, 2007. Female patient was diagnosed with cytomegalovirus infection and was treated with VALACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: foetal disorder, gastrointestinal disorder, hepatomegaly, meconium ileus, ultrasound antenatal screen abnormal, viral load increased, . VALACYCLOVIR dosage: unknown. Patient recovered.

Decadron Side Effects Report #5761303-1
Physician from JAPAN reported DECADRON problem on May 28, 2008. Female patient, 29 years of age, was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: foetal disorder, . DECADRON dosage: unknown. Patient was hospitalized. Patient recovered.

Decadron Side Effects Report #5774088-X
DECADRON problem was reported by a Physician from JAPAN on May 28, 2008. Female patient, 29 years of age, was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: foetal disorder, . DECADRON dosage: unknown. Patient was hospitalized. Patient recovered.


Ondansetron Side Effects Report #5724297-0
Consumer or non-health professional from UNITED KINGDOM reported ONDANSETRON problem on Apr 16, 2008. Female patient was treated with ONDANSETRON. After drug was administered, patient experienced the following problems/side effects: congenital hydronephrosis, foetal disorder, foetal growth retardation, foetal malformation, gastroschisis, heart disease congenital, spinal deformity, . ONDANSETRON dosage: 4 MG, 2 IN 1 D, TRANSPLACENTAL : 4 MG, 3 IN 1 D, TRANSPLACENTAL. During the same period patient was treated with METOCLOPRAMIDE, PROMETHAZINE, THIAMINE, CYCLIZINE, FOLIC ACID. Patient recovered.

Actos Side Effects Report #5345102-0
ACTOS problem was reported by a Consumer or non-health professional from SPAIN on May 24, 2007. Female patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: foetal disorder, hypoglycaemia neonatal, necrotising enterocolitis neonatal, . ACTOS dosage: 30 MG. During the same period patient was treated with GLIMEPIRIDE, LEVOTHYROXINE, INSULIN. Patient recovered.

Pentasa Side Effects Report #5308572-X
Physician from FRANCE reported PENTASA problem on Apr 06, 2007. Female patient was diagnosed with inflammatory bowel disease and was treated with PENTASA. After drug was administered, patient experienced the following problems/side effects: foetal disorder, ultrasound kidney abnormal, . PENTASA dosage: unknown. Patient recovered.

Zyprexa Side Effects Report #5276603-1
ZYPREXA problem was reported by a Physician from JAPAN on Mar 15, 2007. Female patient was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: foetal disorder, . ZYPREXA dosage: 20 MG, DAILY (1/D). Patient recovered.

Clexane Side Effects Report #5677034-2
Pharmacist from GERMANY reported CLEXANE problem on Mar 17, 2008. Female patient, 41 years of age, was diagnosed with pregnancy, migraine and was treated with CLEXANE. After drug was administered, patient experienced the following problems/side effects: caesarean section, foetal disorder, placental insufficiency, pre-eclampsia, . CLEXANE dosage: unknown. Patient recovered.


Cervidil Side Effects Report #5679888-2
CERVIDIL problem was reported by a Consumer or non-health professional from CANADA on Mar 07, 2008. Female patient was treated with CERVIDIL. After drug was administered, patient experienced the following problems/side effects: blood ph decreased, foetal disorder, foetal heart rate abnormal, foetal heart rate deceleration, . CERVIDIL dosage: 10 MG ONCE TRANSPLACENTAL. Patient recovered.

Rebif Side Effects Report #5619651-1
Consumer or non-health professional from UNITED STATES reported REBIF problem on Jan 24, 2008. Female patient, 34 years of age, was diagnosed with multiple sclerosis, depression, neuralgia, balance disorder and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: feeling abnormal, foetal disorder, induced labour, multiple sclerosis, pregnancy, skin discolouration, . REBIF dosage: unknown. During the same period patient was treated with LEXAPRO, NEURONTIN, MECLIZINE. Patient recovered.

Prograf Side Effects Report #5467169-1
PROGRAF problem was reported by a Physician from FRANCE on Sept 07, 2007. Female patient was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: atrioventricular block second degree, foetal disorder, . PROGRAF dosage: unknown. During the same period patient was treated with PREDNISOLONE, ASPIRIN, FERROUS SULPHATE. Patient recovered.

Valacyclovir Side Effects Report #5468184-4
Consumer or non-health professional from FRANCE reported VALACYCLOVIR problem on Sept 10, 2007. Female patient was diagnosed with cytomegalovirus infection and was treated with VALACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: congenital anomaly, foetal disorder, nervous system disorder, premature baby, vascular calcification, . VALACYCLOVIR dosage: unknown. Patient recovered.

Valacyclovir Side Effects Report #5468197-2
VALACYCLOVIR problem was reported by a Consumer or non-health professional from FRANCE on Sept 10, 2007. Female patient was diagnosed with cytomegalovirus infection and was treated with VALACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, foetal disorder, premature baby, splenomegaly, . VALACYCLOVIR dosage: unknown. Patient recovered.

Lexapro Side Effects Report #5695719-9
Physician from UNITED STATES reported LEXAPRO problem on Mar 26, 2008. Female patient was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: bladder disorder, foetal disorder, pregnancy, . LEXAPRO dosage: 20 MG QD TRANSPLACENTAL. During the same period patient was treated with FOLIC ACID, CLONAZEPAM. Patient recovered.

Keppra Side Effects Report #5372521-9
KEPPRA problem was reported by a Physician from UNITED STATES on June 07, 2007. Female patient, weighting 4.19 lb, was diagnosed with epilepsy and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: antepartum haemorrhage, foetal disorder, small for dates baby, . KEPPRA dosage: 500 MG/D TRP. During the same period patient was treated with PRENATAL VITAMINS, FOLIC ACID. Patient recovered.

Teveten Side Effects Report #5325811-X
Pharmacist from UNITED KINGDOM reported TEVETEN problem on Mar 30, 2007. Female patient was treated with TEVETEN. After drug was administered, patient experienced the following problems/side effects: caudal regression syndrome, foetal disorder, hypoperfusion, premature baby, pulmonary hypoplasia, stillbirth, . TEVETEN dosage: 600 MG DAILY PO; A FEW WEEKS. During the same period patient was treated with METFORMIN, BENDROFLUAZIDE. Patient died on 10/22/2006.

Teveten Side Effects Report #5332860-4
TEVETEN problem was reported by a Pharmacist from UNITED KINGDOM on Apr 25, 2007. Female patient, weighting 235.9 lb, was treated with TEVETEN. After drug was administered, patient experienced the following problems/side effects: caudal regression syndrome, foetal disorder, hypoperfusion, pulmonary hypoplasia, stillbirth, . TEVETEN dosage: 600 MG DAILY PO. During the same period patient was treated with METFORMIN, BENDROFLUAZIDE. Patient died.

Keppra Side Effects Report #5279691-1
Consumer or non-health professional from UNITED STATES reported KEPPRA problem on Mar 07, 2007. Female patient, 37 years of age, was diagnosed with epilepsy and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: biopsy chorionic villous abnormal, foetal disorder, trisomy 18, twin pregnancy, . KEPPRA dosage: 1750 MG/D PO. During the same period patient was treated with PHENOBARBITAL, PRENATAL VITAMINS, FOLIC ACID. Patient recovered.