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

ASTHENIA ( 3 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PAIN ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
DEATH ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
COMA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
AUTISM ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
ANGER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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