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

RASH ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
FALL ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SNORING ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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