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

HEART RATE INCREASED ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
INFECTION ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
PYREXIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TENSION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
CRIME ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
COLITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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