Please choose an event type to view the corresponding MedsFacts report:

DRUG INEFFECTIVE ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
PROTEINURIA ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
FALL ( 4 FDA reports)
ANORGASMIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FAILED INDUCTION OF LABOUR ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
COLITIS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
APHONIA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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