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Paxil Side Effects Report #5601252-2
Consumer or non-health professional from UNITED STATES reported PAXIL problem on Jan 17, 2008. Male patient was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: breech presentation, dyspnoea, heart disease congenital, premature baby, pulmonary malformation, . PAXIL dosage: 40MG TWICE PER DAY. During the same period patient was treated with PRENATAL VITAMINS. Patient recovered.

Prograf Side Effects Report #5573974-3
PROGRAF problem was reported by a Physician from UNITED STATES on Dec 04, 2007. Female patient, 38 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: breech presentation, pregnancy, . PROGRAF dosage: unknown. Patient recovered.

Prograf Side Effects Report #5573976-7
Physician from UNITED STATES reported PROGRAF problem on Dec 04, 2007. Female patient, 25 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, pregnancy, . PROGRAF dosage: unknown. Patient recovered.

Leponex Side Effects Report #5477900-7
LEPONEX problem was reported by a Physician from GERMANY on Oct 01, 2007. Female patient, 28 years of age, was diagnosed with schizophrenia, depression and was treated with LEPONEX. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, . LEPONEX dosage: 150 MG/DAY. During the same period patient was treated with FLUOXETINE, ZOLPIDEM TARTRATE. Patient was hospitalized. Patient recovered.


Truvada Side Effects Report #5442683-3
Consumer or non-health professional from UNITED STATES reported TRUVADA problem on Aug 29, 2007. Female patient, weighting 2.70 lb, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, multiple congenital abnormalities, stillbirth, umbilical cord abnormality, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, VIRAMUNE. Patient died on 07/04/2007.

Truvada Side Effects Report #5404190-3
TRUVADA problem was reported by a Consumer or non-health professional from UNITED STATES on July 23, 2007. Female patient, weighting 2.70 lb, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, multiple congenital abnormalities, stillbirth, umbilical cord abnormality, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, VIRAMUNE. Patient died on 07/04/2007.

Truvada Side Effects Report #5411448-0
Consumer or non-health professional from UNITED STATES reported TRUVADA problem on July 31, 2007. Female patient, weighting 2.70 lb, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, multiple congenital abnormalities, stillbirth, umbilical cord abnormality, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, VIRAMUNE. Patient died on 07/04/2007.

Methotrexate Side Effects Report #5412744-3
METHOTREXATE problem was reported by a Physician from UNITED STATES on July 24, 2007. Female patient was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, congenital anomaly, congenital tongue anomaly, developmental delay, dubowitz syndrome, dysmorphism, . METHOTREXATE dosage: 50 MG/M2, SINGLE, TRANSPLACENTAL. During the same period patient was treated with MISOPROSTOL. Patient recovered.

Sustiva Side Effects Report #5417028-5
Health Professional from UNITED STATES reported SUSTIVA problem on July 20, 2007. Female patient, 31 years of age, was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, foetal malformation, oligohydramnios, pregnancy, stillbirth, umbilical cord abnormality, . SUSTIVA dosage: unknown. During the same period patient was treated with TRUVADA, VIRAMUNE. Patient recovered.


Sustiva Side Effects Report #5423492-8
SUSTIVA problem was reported by a Health Professional from UNITED STATES on Aug 09, 2007. Female patient, 31 years of age, was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, foetal malformation, oligohydramnios, pregnancy, stillbirth, umbilical cord abnormality, . SUSTIVA dosage: unknown. During the same period patient was treated with TRUVADA, VIRAMUNE, BACTRIM. Patient recovered.

Truvada Side Effects Report #5383586-2
Consumer or non-health professional from UNITED STATES reported TRUVADA problem on July 06, 2007. Female patient, weighting 2.70 lb, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, multiple congenital abnormalities, stillbirth, umbilical cord abnormality, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, VIRAMUNE. Patient died on 07/04/2007.

Sustiva Side Effects Report #5386362-X
SUSTIVA problem was reported by a Health Professional from UNITED STATES on July 06, 2007. Female patient, 31 years of age, was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, foetal malformation, oligohydramnios, stillbirth, umbilical cord abnormality, . SUSTIVA dosage: unknown. During the same period patient was treated with TRUVADA, VIRAMUNE. Patient recovered.

Isotretinoin Side Effects Report #5387175-5
Physician from UNITED STATES reported ISOTRETINOIN problem on June 27, 2007. Female patient, 19 years of age, was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: breech presentation, pregnancy, . ISOTRETINOIN dosage: 40 MG, QD, ORAL. Patient recovered.

Truvada Side Effects Report #5394678-6
TRUVADA problem was reported by a Consumer or non-health professional from UNITED STATES on July 16, 2007. Female patient, weighting 2.70 lb, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, multiple congenital abnormalities, stillbirth, umbilical cord abnormality, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, VIRAMUNE. Patient died on 07/04/2007.


Leponex Side Effects Report #5399832-5
Physician from GERMANY reported LEPONEX problem on July 23, 2007. Female patient, 28 years of age, was diagnosed with schizophrenia, depression and was treated with LEPONEX. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, . LEPONEX dosage: 150 MG/DAY. During the same period patient was treated with FLUOXETINE, ZOLPIDEM TARTRATE. Patient was hospitalized. Patient recovered.

Truvada Side Effects Report #5383586-2
TRUVADA problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, weighting 2.70 lb, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, multiple congenital abnormalities, stillbirth, umbilical cord abnormality, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, VIRAMUNE. Patient died on 07/04/2007.

Sustiva Side Effects Report #5386362-X
Health Professional from UNITED STATES reported SUSTIVA problem on July 06, 2007. Female patient, 31 years of age, was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, foetal malformation, oligohydramnios, stillbirth, umbilical cord abnormality, . SUSTIVA dosage: unknown. During the same period patient was treated with TRUVADA, VIRAMUNE. Patient recovered.

Isotretinoin Side Effects Report #5387175-5
ISOTRETINOIN problem was reported by a Physician from UNITED STATES on June 27, 2007. Female patient, 19 years of age, was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: breech presentation, pregnancy, . ISOTRETINOIN dosage: 40 MG, QD, ORAL. Patient recovered.

Truvada Side Effects Report #5394678-6
Consumer or non-health professional from UNITED STATES reported TRUVADA problem on July 16, 2007. Female patient, weighting 2.70 lb, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: breech presentation, dandy-walker syndrome, foetal growth retardation, multiple congenital abnormalities, stillbirth, umbilical cord abnormality, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, VIRAMUNE. Patient died on 07/04/2007.


Leponex Side Effects Report #5399832-5
LEPONEX problem was reported by a Physician from GERMANY on July 23, 2007. Female patient, 28 years of age, was diagnosed with schizophrenia, depression and was treated with LEPONEX. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, . LEPONEX dosage: 150 MG/DAY. During the same period patient was treated with FLUOXETINE, ZOLPIDEM TARTRATE. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5780281-2
Health Professional from SWEDEN reported REMICADE problem on June 10, 2008. Female patient, weighting 125.7 lb, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: breech presentation, premature rupture of membranes, . REMICADE dosage: unknown. During the same period patient was treated with IMUREL. Patient recovered.

Vitamin Side Effects Report #5728359-3
VITAMIN problem was reported by a Physician from UNITED STATES on Apr 30, 2008. Female patient, 32 years of age, was diagnosed with blood prolactin increased and was treated with VITAMIN. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, convulsion, normal newborn, . VITAMIN dosage: unknown. During the same period patient was treated with FOLIC ACID, PARLODEL. Patient recovered.

Paxil Side Effects Report #5730565-9
Physician from UNITED STATES reported PAXIL problem on Apr 29, 2008. Male patient was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: breech presentation, dyspnoea, heart disease congenital, premature baby, pulmonary malformation, . PAXIL dosage: 40MG TWICE PER DAY. During the same period patient was treated with VITAMIN, ABILIFY. Patient recovered.

Claravis Side Effects Report #5731706-X
CLARAVIS problem was reported by a Health Professional from UNITED STATES on Apr 21, 2008. Female patient, 22 years of age, weighting 125.0 lb, was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, cystitis, pregnancy on oral contraceptive, treatment noncompliance, unintended pregnancy, . CLARAVIS dosage: 40 MG, BID, ORAL; 40 MG, BID, ORAL. Patient was hospitalized. Patient recovered.

Claravis Side Effects Report #5752390-5
Physician from UNITED STATES reported CLARAVIS problem on May 07, 2008. Female patient was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, foetal growth retardation, premature baby, small for dates baby, . CLARAVIS dosage: 40 MG, BID, TRANSPLACENTAL. Patient recovered.

Claravis Side Effects Report #5752430-3
CLARAVIS problem was reported by a Health Professional from UNITED STATES on May 07, 2008. Female patient, 22 years of age, weighting 125.0 lb, was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, cystitis, pregnancy on oral contraceptive, pregnancy with contraceptive device, premature rupture of membranes, treatment noncompliance, unintended pregnancy, . CLARAVIS dosage: 40MG, BID, ORAL. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5692666-3
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 19, 2008. Female patient, 32 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, incision site complication, pregnancy, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5692692-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 19, 2008. Male patient was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, . AVONEX dosage: unknown. Patient recovered.

Metronidazol Side Effects Report #5701287-5
Physician from GERMANY reported METRONIDAZOL HEXAL problem on Mar 28, 2008. Female patient, weighting 138.9 lb, was diagnosed with vaginitis bacterial and was treated with METRONIDAZOL HEXAL. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, . METRONIDAZOL HEXAL dosage: 400 MG, BID, ORAL. Patient recovered.

Avonex Side Effects Report #5712500-2
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 11, 2008. Female patient, 32 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, pregnancy, scar pain, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5712825-0
Consumer or non-health professional from UNITED STATES reported PAXIL problem on Apr 09, 2008. Male patient was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: breech presentation, dyspnoea, heart disease congenital, premature baby, pulmonary malformation, . PAXIL dosage: 40MG TWICE PER DAY. During the same period patient was treated with VITAMIN. Patient recovered.

Salbutamol Side Effects Report #5713287-X
SALBUTAMOL problem was reported by a Physician from GREECE on Apr 04, 2008. Female patient, 23 years of age, was diagnosed with tocolysis and was treated with SALBUTAMOL. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, delayed delivery, gestational diabetes, oligohydramnios, premature labour, premature rupture of membranes, twin pregnancy, . SALBUTAMOL dosage: 12 MG; ORAL. Patient recovered.

Claravis Side Effects Report #5366069-5
Consumer or non-health professional from UNITED STATES reported CLARAVIS problem on June 05, 2007. Female patient, 29 years of age, was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, pregnancy, . CLARAVIS dosage: 40 MG BID ORAL. Patient recovered.

Femara Side Effects Report #5375335-9
FEMARA problem was reported by a Consumer or non-health professional from CANADA on June 22, 2007. Female patient, 26 years of age, weighting 142.9 lb, was diagnosed with ovulation induction and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, normal newborn, . FEMARA dosage: 2.5 MG ONCE A DAY FOR 5 DAYS. Patient was hospitalized. Patient recovered.

Femara Side Effects Report #5375345-1
Consumer or non-health professional from CANADA reported FEMARA problem on June 22, 2007. Female patient, 26 years of age, weighting 142.9 lb, was diagnosed with ovulation induction and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, normal newborn, . FEMARA dosage: 2.5 MG ONCE A DAY FOR 5 DAYS. Patient was hospitalized. Patient recovered.

Propecia Side Effects Report #5318414-4
PROPECIA problem was reported by a Physician from UNITED KINGDOM on Apr 30, 2007. Female patient, weighting 6.61 lb, was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: breech presentation, . PROPECIA dosage: unknown. Patient was hospitalized. Patient recovered.

Escitalopram Side Effects Report #5319596-0
Health Professional from FINLAND reported ESCITALOPRAM problem on Apr 20, 2007. Male patient, weighting 6.80 lb, was diagnosed with depression and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, congenital hand malformation, dysmorphism, . ESCITALOPRAM dosage: 10 MG QD TRANSPLACENTAL. During the same period patient was treated with XENICAL, SELEXID, SUCRALFATE, AGIOCUR, LAXOBERON, LANSOPRAZOLE, TOLTERODINE TARTRATE. Patient recovered.

Isotretinoin Side Effects Report #5343884-5
ISOTRETINOIN problem was reported by a Physician from UNITED STATES on May 17, 2007. Female patient, 19 years of age, was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: breech presentation, pregnancy, . ISOTRETINOIN dosage: 40 MG, QD, ORAL. Patient recovered.

Escitalopram Side Effects Report #5298376-9
Consumer or non-health professional from FINLAND reported ESCITALOPRAM problem on Mar 22, 2007. Male patient was diagnosed with depression and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, congenital anomaly, dysmorphism, . ESCITALOPRAM dosage: 10 MG QD TRANSPLACENTAL. During the same period patient was treated with XENICAL, SELEXID, SUCRALFATE, AGIOCUR, LAXOBERON, LANZOPRATSOL, TOLTERODINE TARTRATE. Patient recovered.

Escitalopram Side Effects Report #5308985-6
ESCITALOPRAM problem was reported by a Health Professional from FINLAND on Apr 04, 2007. Male patient, weighting 6.80 lb, was diagnosed with depression and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, congenital hand malformation, dysmorphism, . ESCITALOPRAM dosage: 10 MG QD TRANSPLACENTAL. During the same period patient was treated with XENICAL, SELEXID, SUCRALFATE, AGIOCUR, LAXOBERON, LANZOPRATSOL, TOLTERODINE TARTRATE. Patient recovered.

Imatinib Side Effects Report #5267144-6
Health Professional from SINGAPORE reported IMATINIB MESYLATE problem on Mar 05, 2007. Female patient, 36 years of age, was diagnosed with chronic myeloid leukaemia and was treated with IMATINIB MESYLATE. After drug was administered, patient experienced the following problems/side effects: breech presentation, caesarean section, normal newborn, . IMATINIB MESYLATE dosage: 600 MG/D. During the same period patient was treated with IMATINIB MESYLATE, INTERFERON ALFA, INTERFERON ALFA. Patient recovered.

Paxil Side Effects Report #5651017-0
PAXIL CR problem was reported by a Pharmacist from UNITED STATES on Feb 15, 2008. Male patient, weighting 6.61 lb, was diagnosed with depression and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: atrial septal defect, breech presentation, cardiac failure congestive, cardiac murmur, cardiomegaly, cyanosis, failure to thrive, heart disease congenital, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with VITAMIN, MOTRIN, ALEVE, ZANTAC, PREVACID, AMOXICILLIN, NAPROXEN. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5669398-0
Pharmacist from UNITED STATES reported PAXIL CR problem on Feb 29, 2008. Male patient, weighting 6.61 lb, was diagnosed with depression and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: atrial septal defect, breech presentation, cardiac failure congestive, cardiac murmur, cardiomegaly, cyanosis, failure to thrive, heart disease congenital, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with VITAMIN, MOTRIN, ALEVE, ZANTAC, PREVACID, AMOXICILLIN, NAPROXEN, BUPAP. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5672859-1
PAXIL CR problem was reported by a Pharmacist from UNITED STATES on Mar 04, 2008. Male patient, weighting 6.61 lb, was diagnosed with depression and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: atrial septal defect, breech presentation, cardiac failure congestive, cardiac murmur, cardiomegaly, cyanosis, failure to thrive, heart disease congenital, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with VITAMIN, MOTRIN, ALEVE, ZANTAC, PREVACID, AMOXICILLIN, NAPROXEN, BUPAP. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5618457-7
Pharmacist from UNITED STATES reported PAXIL CR problem on Jan 28, 2008. Male patient, weighting 6.61 lb, was diagnosed with depression and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: atrial septal defect, breech presentation, cardiac failure congestive, cardiac murmur, cardiomegaly, cyanosis, failure to thrive, heart disease congenital, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with PRENATAL VITAMINS, MOTRIN, ALEVE, ZANTAC, PREVACID, AMOXICILLIN, NAPROXEN. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5640860-X
PAXIL CR problem was reported by a Pharmacist from UNITED STATES on Feb 11, 2008. Male patient, weighting 6.61 lb, was diagnosed with depression and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: atrial septal defect, breech presentation, cardiac failure congestive, cardiac murmur, cardiomegaly, cyanosis, failure to thrive, heart disease congenital, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with VITAMIN, MOTRIN, ALEVE, ZANTAC, PREVACID, AMOXICILLIN, NAPROXEN. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5645300-2
Pharmacist from UNITED STATES reported PAXIL CR problem on Feb 14, 2008. Male patient, weighting 6.61 lb, was diagnosed with depression and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: atrial septal defect, breech presentation, cardiac failure congestive, cardiac murmur, cardiomegaly, cyanosis, failure to thrive, heart disease congenital, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with VITAMIN, MOTRIN, ALEVE, ZANTAC, PREVACID, AMOXICILLIN, NAPROXEN. Patient was hospitalized. Patient recovered.

Reyataz Side Effects Report #5608165-0
REYATAZ problem was reported by a Physician from FRANCE on Jan 25, 2008. Male patient, weighting 4.41 lb, was treated with REYATAZ. After drug was administered, patient experienced the following problems/side effects: atrophy, breech presentation, foetal growth retardation, . REYATAZ dosage: unknown. During the same period patient was treated with TRUVADA, NORVIR. Patient recovered.

Paxil Side Effects Report #5525508-7
Pharmacist from UNITED STATES reported PAXIL CR problem on Nov 15, 2007. Male patient, weighting 6.61 lb, was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: atrial septal defect, breech presentation, cardiac failure congestive, cardiac murmur, cardiomegaly, cyanosis, failure to thrive, heart disease congenital, . PAXIL CR dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS, MOTRIN, ALEVE, ZANTAC. Patient was hospitalized. Patient recovered.

Aldomet Side Effects Report #5490839-6
ALDOMET problem was reported by a Physician from JAPAN on Oct 10, 2007. Female patient, 21 years of age, was treated with ALDOMET. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, breech presentation, glomerulonephritis chronic, protein urine present, . ALDOMET dosage: unknown. Patient was hospitalized. Patient recovered.

Aldomet Side Effects Report #5403342-6
Physician from JAPAN reported ALDOMET problem on July 25, 2007. Female patient, 21 years of age, was treated with ALDOMET. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, breech presentation, glomerulonephritis chronic, protein urine present, . ALDOMET dosage: unknown. Patient was hospitalized. Patient recovered.